Linked Data
ClinVar Variation Id:
2938865
ClinVar RCV Id:
RCV003799639
dbSNP Id:
rs1210477192
gnomAD v3:
1-201065850-G-T
gnomAD v4:
1-201065850-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.201065850G>T , CM000663.2:g.201065850G>T | GRCh38 |
| NC_000001.10:g.201034978G>T , CM000663.1:g.201034978G>T | GRCh37 |
| NC_000001.9:g.199301601G>T | NCBI36 |
| NG_009816.1:g.51717C>A | |
| NG_009816.2:g.51717C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000362061.4:c.2841C>A MANE Select | ENSP00000355192.3:p.Val947= | |
| ENST00000679417.1:c.*2004C>A | ENSP00000506706.1:n.*2004C>A | |
| ENST00000680059.1:c.*359C>A | ENSP00000504944.1:n.*359C>A | |
| ENST00000681078.1:c.2841C>A | ENSP00000506645.1:p.Val947= | |
| ENST00000681190.1:c.2841C>A | ENSP00000506428.1:p.Val947= | |
| ENST00000681874.1:c.2781C>A | ENSP00000505162.1:p.Val927= | |
| ENST00000362061.3:c.2841C>A | ENSP00000355192.3:p.Val947= | |
| ENST00000367338.7:c.2841C>A | ENSP00000356307.3:p.Val947= | |
| NM_000069.2:c.2841C>A | NP_000060.2:p.Val947= | |
| XM_005245478.2:c.2841C>A | XP_005245535.1:p.Val947= | |
| XM_005245478.3:c.2841C>A | XP_005245535.1:p.Val947= | |
| NM_000069.3:c.2841C>A MANE Select | NP_000060.2:p.Val947= |