Linked Data
ClinVar Variation Id:
1146731
ClinVar RCV Id:
RCV001486028
dbSNP Id:
rs1193232549
gnomAD v4:
7-92499788-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.92499788C>T , CM000669.2:g.92499788C>T | GRCh38 |
| NC_000007.13:g.92129102C>T , CM000669.1:g.92129102C>T | GRCh37 |
| NC_000007.12:g.91967038C>T | NCBI36 |
| NG_008341.1:g.33744G>A | |
| NG_008341.2:g.33744G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248633.9:c.2634G>A MANE Select | ENSP00000248633.4:p.Leu878= | |
| ENST00000248633.8:c.2634G>A | ENSP00000248633.4:p.Leu878= | |
| ENST00000428214.5:c.2463G>A | ENSP00000394413.1:p.Leu821= | |
| ENST00000438045.5:c.1668G>A | ENSP00000410438.1:p.Leu556= | |
| ENST00000484913.5:n.2673G>A | ||
| ENST00000496420.5:n.2526G>A | ||
| NM_000466.2:c.2634G>A | NP_000457.1:p.Leu878= | |
| NM_001282677.1:c.2463G>A | NP_001269606.1:p.Leu821= | |
| NM_001282678.1:c.2010G>A | NP_001269607.1:p.Leu670= | |
| XM_005250433.3:c.885G>A | XP_005250490.1:p.Leu295= | |
| XR_242246.3:n.2730G>A | ||
| XM_017012319.2:c.885G>A | XP_016867808.1:p.Leu295= | |
| XR_001744808.2:n.1661G>A | ||
| XR_242246.5:n.2681G>A | ||
| NM_000466.3:c.2634G>A MANE Select | NP_000457.1:p.Leu878= | |
| NM_001282677.2:c.2463G>A | NP_001269606.1:p.Leu821= | |
| NM_001282678.2:c.2010G>A | NP_001269607.1:p.Leu670= |