SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
Linked Data
MyVariant Identifiers:
chr3:g.12632380G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.12590881G>T , CM000665.2:g.12590881G>T | GRCh38 |
| NC_000003.11:g.12632380G>T , CM000665.1:g.12632380G>T | GRCh37 |
| NC_000003.10:g.12607380G>T | NCBI36 |
| NG_007467.1:g.78299C>A , LRG_413:g.78299C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000423275.6:c.*952C>A | ENSP00000401088.1:n.*952C>A | |
| ENST00000432427.3:c.604C>A | ||
| ENST00000460610.2:n.81C>A | ||
| ENST00000465826.6:n.878C>A | ||
| ENST00000475353.2:n.1209C>A | ||
| ENST00000494557.2:n.1098C>A | ||
| ENST00000684903.1:c.*964C>A | ENSP00000508612.1:n.*964C>A | |
| ENST00000685348.1:c.*964C>A | ENSP00000510285.1:n.*964C>A | |
| ENST00000685437.1:c.1188C>A | ENSP00000508794.1:p.Leu396= | |
| ENST00000685653.1:c.1287C>A | ENSP00000509968.1:p.Leu429= | |
| ENST00000685738.1:c.*251C>A | ENSP00000510156.1:n.*251C>A | |
| ENST00000686409.1:n.2338C>A | ||
| ENST00000686455.1:n.1650C>A | ||
| ENST00000686762.1:c.1287C>A | ENSP00000509767.1:p.Leu429= | |
| ENST00000687257.1:n.1523C>A | ||
| ENST00000687326.1:c.*221C>A | ENSP00000509665.1:n.*221C>A | |
| ENST00000687505.1:n.1405C>A | ||
| ENST00000687923.1:c.1176C>A | ENSP00000510255.1:p.Leu392= | |
| ENST00000687940.1:n.1664C>A | ||
| ENST00000688269.1:n.1883C>A | ||
| ENST00000688326.1:c.720C>A | ||
| ENST00000688444.1:n.1613C>A | ||
| ENST00000688543.1:c.1188C>A | ENSP00000509612.1:p.Leu396= | |
| ENST00000688625.1:c.*865C>A | ENSP00000509522.1:n.*865C>A | |
| ENST00000688803.1:n.1518C>A | ||
| ENST00000688914.1:n.273C>A | ||
| ENST00000689097.1:c.*964C>A | ENSP00000509756.1:n.*964C>A | |
| ENST00000689389.1:c.1193+827C>A | ENSP00000510213.1:n.1193+827C>A | |
| ENST00000689418.1:c.*964C>A | ENSP00000509467.1:n.*964C>A | |
| ENST00000689481.1:c.*964C>A | ENSP00000510248.1:n.*964C>A | |
| ENST00000689540.1:n.1437C>A | ||
| ENST00000689876.1:c.1287C>A | ENSP00000508535.1:p.Leu429= | |
| ENST00000689914.1:c.*221C>A | ENSP00000509847.1:n.*221C>A | |
| ENST00000690397.1:c.1176C>A | ENSP00000508730.1:p.Leu392= | |
| ENST00000690460.1:c.1275C>A | ENSP00000509106.1:p.Leu425= | |
| ENST00000690585.1:c.179C>A | ||
| ENST00000690625.1:n.2323C>A | ||
| ENST00000691396.1:c.*1139C>A | ENSP00000510712.1:n.*1139C>A | |
| ENST00000691724.1:c.*244C>A | ENSP00000509255.1:n.*244C>A | |
| ENST00000691779.1:c.*865C>A | ENSP00000508592.1:n.*865C>A | |
| ENST00000691888.1:c.179C>A | ||
| ENST00000691899.1:c.1287C>A | ENSP00000508763.1:p.Leu429= | |
| ENST00000692069.1:n.1853C>A | ||
| ENST00000692093.1:c.1188C>A | ENSP00000509669.1:p.Leu396= | |
| ENST00000692311.1:n.2111C>A | ||
| ENST00000692558.1:n.1652C>A | ||
| ENST00000692773.1:c.*1024C>A | ENSP00000509055.1:n.*1024C>A | |
| ENST00000692830.1:c.*1032C>A | ENSP00000509461.1:n.*1032C>A | |
| ENST00000693069.1:c.*221C>A | ENSP00000510072.1:n.*221C>A | |
| ENST00000693312.1:c.1062C>A | ENSP00000508686.1:p.Leu354= | |
| ENST00000693664.1:c.1287C>A | ENSP00000509614.1:p.Leu429= | |
| ENST00000693705.1:c.*964C>A | ENSP00000510697.1:n.*964C>A | |
| ENST00000251849.9:c.1287C>A MANE Select | ENSP00000251849.4:p.Leu429= | |
| ENST00000442415.7:c.1347C>A | ENSP00000401888.2:p.Leu449= | |
| ENST00000251849.8:c.1287C>A | ENSP00000251849.4:p.Leu429= | |
| ENST00000423275.5:c.*964C>A | ENSP00000401088.1:n.*964C>A | |
| ENST00000432427.2:c.924C>A | ENSP00000398591.2:p.Leu308= | |
| ENST00000442415.6:c.1347C>A | ENSP00000401888.2:p.Leu449= | |
| ENST00000460610.1:n.244C>A | ||
| ENST00000465826.5:n.644C>A | ||
| ENST00000475353.1:n.455C>A | ||
| ENST00000494557.1:n.303C>A | ||
| NM_002880.3:c.1287C>A , LRG_413t1:c.1287C>A | NP_002871.1:p.Leu429= | |
| XM_005265355.1:c.1287C>A | XP_005265412.1:p.Leu429= | |
| XM_005265357.1:c.1188C>A | XP_005265414.1:p.Leu396= | |
| XM_005265358.3:c.1044C>A | XP_005265415.1:p.Leu348= | |
| XM_005265359.3:c.945C>A | XP_005265416.1:p.Leu315= | |
| XM_005265360.1:c.1287C>A | XP_005265417.1:p.Leu429= | |
| XM_011533974.1:c.1287C>A | XP_011532276.1:p.Leu429= | |
| XM_011533975.1:c.1044C>A | XP_011532277.1:p.Leu348= | |
| NM_001354689.1:c.1347C>A | NP_001341618.1:p.Leu449= | |
| NM_001354690.1:c.1287C>A | NP_001341619.1:p.Leu429= | |
| NM_001354691.1:c.1044C>A | NP_001341620.1:p.Leu348= | |
| NM_001354692.1:c.1044C>A | NP_001341621.1:p.Leu348= | |
| NM_001354693.1:c.1188C>A | NP_001341622.1:p.Leu396= | |
| NM_001354694.1:c.1104C>A | NP_001341623.1:p.Leu368= | |
| NM_001354695.1:c.945C>A | NP_001341624.1:p.Leu315= | |
| NR_148940.1:n.1815C>A | ||
| NR_148941.1:n.1761C>A | ||
| NR_148942.1:n.1700C>A | ||
| XM_011533974.3:c.1287C>A | XP_011532276.1:p.Leu429= | |
| XM_017006966.1:c.1188C>A | XP_016862455.1:p.Leu396= | |
| NM_001354689.3:c.1347C>A | NP_001341618.1:p.Leu449= | |
| NM_001354690.2:c.1287C>A | NP_001341619.1:p.Leu429= | |
| NM_001354691.2:c.1044C>A | NP_001341620.1:p.Leu348= | |
| NM_001354692.2:c.1044C>A | NP_001341621.1:p.Leu348= | |
| NM_001354693.2:c.1188C>A | NP_001341622.1:p.Leu396= | |
| NM_001354694.2:c.1104C>A | NP_001341623.1:p.Leu368= | |
| NM_001354695.2:c.945C>A | NP_001341624.1:p.Leu315= | |
| NR_148940.2:n.1731C>A | ||
| NR_148941.2:n.1677C>A | ||
| NR_148942.2:n.1616C>A | ||
| NM_001354690.3:c.1287C>A | NP_001341619.1:p.Leu429= | |
| NM_001354691.3:c.1044C>A | NP_001341620.1:p.Leu348= | |
| NM_001354692.3:c.1044C>A | NP_001341621.1:p.Leu348= | |
| NM_001354693.3:c.1188C>A | NP_001341622.1:p.Leu396= | |
| NM_001354694.3:c.1104C>A | NP_001341623.1:p.Leu368= | |
| NM_001354695.3:c.945C>A | NP_001341624.1:p.Leu315= | |
| NM_002880.4:c.1287C>A MANE Select | NP_002871.1:p.Leu429= | |
| NR_148940.3:n.1731C>A | ||
| NR_148941.3:n.1677C>A | ||
| NR_148942.3:n.1616C>A |