Linked Data
ClinVar Variation Id:
1094420
ClinVar RCV Id:
RCV001414957
dbSNP Id:
rs749324210
gnomAD v4:
8-144515059-C-A
MyVariant Identifiers:
chr8:g.145740443C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.144515059C>A , CM000670.2:g.144515059C>A | GRCh38 |
| NC_000008.10:g.145740443C>A , CM000670.1:g.145740443C>A | GRCh37 |
| NC_000008.9:g.145711251C>A | NCBI36 |
| NG_016430.1:g.7768G>T | |
| NG_033083.1:g.2095C>A | |
| NG_016430.2:g.7768G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000688394.1:n.520G>T | ||
| ENST00000617875.6:c.1497G>T MANE Select | ENSP00000482313.2:p.Leu499= | |
| ENST00000532846.2:c.369-17G>T | ||
| ENST00000617875.4:c.1497G>T | ENSP00000482313.1:p.Leu499= | |
| ENST00000621189.4:c.426G>T | ENSP00000483145.1:p.Leu142= | |
| NM_004260.3:c.1497G>T | NP_004251.3:p.Leu499= | |
| XM_011517380.1:c.1497G>T | XP_011515682.1:p.Leu499= | |
| XM_011517381.1:c.1401G>T | XP_011515683.1:p.Leu467= | |
| XM_011517382.1:c.1497G>T | XP_011515684.1:p.Leu499= | |
| XM_011517383.1:c.1497G>T | XP_011515685.1:p.Leu499= | |
| XM_011517384.1:c.1497G>T | XP_011515686.1:p.Leu499= | |
| XM_011517385.1:c.360G>T | XP_011515687.1:p.Leu120= | |
| XR_928366.1:n.1538G>T | ||
| XR_928367.1:n.1538G>T | ||
| XR_928368.1:n.1540G>T | ||
| XM_011517384.3:c.1497G>T | XP_011515686.1:p.Leu499= | |
| XM_017013991.2:c.1497G>T | XP_016869480.1:p.Leu499= | |
| XM_017013992.2:c.1497G>T | XP_016869481.1:p.Leu499= | |
| XM_017013993.2:c.1497G>T | XP_016869482.1:p.Leu499= | |
| XM_017013994.2:c.1401G>T | XP_016869483.1:p.Leu467= | |
| XM_017013995.2:c.1497G>T | XP_016869484.1:p.Leu499= | |
| XM_017013996.2:c.1497G>T | XP_016869485.1:p.Leu499= | |
| XM_017013997.2:c.1497G>T | XP_016869486.1:p.Leu499= | |
| XM_017013998.1:c.1497G>T | XP_016869487.1:p.Leu499= | |
| XM_017013999.2:c.1497G>T | XP_016869488.1:p.Leu499= | |
| XM_017014000.1:c.360G>T | XP_016869489.1:p.Leu120= | |
| XM_017014001.2:c.360G>T | XP_016869490.1:p.Leu120= | |
| XR_001745626.2:n.1534G>T | ||
| XR_001745627.2:n.1534G>T | ||
| XR_001745628.2:n.1534G>T | ||
| XR_001745629.2:n.1534G>T | ||
| XR_001745630.2:n.1534G>T | ||
| NM_004260.4:c.1497G>T MANE Select | NP_004251.4:p.Leu499= |