Linked Data
ClinVar Variation Id:
1410900
ClinVar RCV Id:
RCV001918706
dbSNP Id:
rs929097201
gnomAD v3:
19-40395967-C-T
gnomAD v4:
19-40395967-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.40395967C>T , CM000681.2:g.40395967C>T | GRCh38 |
| NC_000019.9:g.40901874C>T , CM000681.1:g.40901874C>T | GRCh37 |
| NC_000019.8:g.45593714C>T | NCBI36 |
| NG_007979.1:g.22398G>A , LRG_265:g.22398G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000324001.8:c.2385G>A MANE Select | ENSP00000326018.6:p.Met795Ile | |
| ENST00000673881.1:c.1968G>A | ENSP00000501070.1:p.Met656Ile | |
| ENST00000674005.2:c.2670G>A | ENSP00000501261.1:p.Met890Ile | |
| ENST00000674773.1:c.1968G>A | ENSP00000502579.1:p.Met656Ile | |
| ENST00000675517.1:c.2260G>A | ||
| ENST00000676076.1:c.2246G>A | ||
| ENST00000676260.1:c.2347G>A | ||
| ENST00000676316.1:c.2272G>A | ||
| ENST00000291825.11:c.*2590G>A | ENSP00000291825.6:n.*2590G>A | |
| ENST00000324001.7:c.2385G>A | ENSP00000326018.6:p.Met795Ile | |
| NM_020956.2:c.*2590G>A , LRG_265t1:c.*2590G>A | NP_066007.1:n.*2590G>A | |
| NM_181882.2:c.2385G>A , LRG_265t2:c.2385G>A | NP_870998.2:p.Met795Ile | |
| XM_011527171.1:c.2385G>A | XP_011525473.1:p.Met795Ile | |
| XM_011527171.2:c.2385G>A | XP_011525473.1:p.Met795Ile | |
| XM_017027046.1:c.2283G>A | XP_016882535.1:p.Met761Ile | |
| XM_017027047.1:c.2283G>A | XP_016882536.1:p.Met761Ile | |
| NM_181882.3:c.2385G>A MANE Select | NP_870998.2:p.Met795Ile |