Linked Data
ClinVar Variation Id:
16265
ClinVar RCV Id:
RCV000017653
dbSNP Id:
rs121909654
gnomAD v4:
5-180619680-C-T
PubMed:
PMID:16965327
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.180619680C>T , CM000667.2:g.180619680C>T | GRCh38 |
| NC_000005.9:g.180046680C>T , CM000667.1:g.180046680C>T | GRCh37 |
| NC_000005.8:g.179979286C>T | NCBI36 |
| NG_011536.1:g.34945G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261937.11:c.2632G>A MANE Select | ENSP00000261937.6:p.Val878Met | |
| ENST00000261937.10:c.2632G>A | ENSP00000261937.6:p.Val878Met | |
| ENST00000393347.7:c.2632G>A | ENSP00000377016.3:p.Val878Met | |
| ENST00000502649.5:c.2632G>A | ENSP00000426057.1:p.Val878Met | |
| ENST00000507059.5:n.1727G>A | ||
| ENST00000619105.4:c.*1575G>A | ENSP00000481134.1:n.*1575G>A | |
| NM_002020.4:c.2632G>A | NP_002011.2:p.Val878Met | |
| NM_182925.4:c.2632G>A | NP_891555.2:p.Val878Met | |
| XM_011534477.1:c.2881G>A | XP_011532779.1:p.Val961Met | |
| XM_011534478.1:c.2863G>A | XP_011532780.1:p.Val955Met | |
| XM_011534479.1:c.2881G>A | XP_011532781.1:p.Val961Met | |
| XM_011534480.1:c.2881G>A | XP_011532782.1:p.Val961Met | |
| XM_011534481.1:c.2881G>A | XP_011532783.1:p.Val961Met | |
| XM_011534482.1:c.2650G>A | XP_011532784.1:p.Val884Met | |
| XM_011534483.1:c.2572G>A | XP_011532785.1:p.Val858Met | |
| XM_011534484.1:c.2173G>A | XP_011532786.1:p.Val725Met | |
| XR_941095.1:n.2893G>A | ||
| NM_001354989.1:c.2632G>A | NP_001341918.1:p.Val878Met | |
| XM_011534478.3:c.2863G>A | XP_011532780.1:p.Val955Met | |
| XM_011534484.2:c.2173G>A | XP_011532786.1:p.Val725Met | |
| XM_017009263.1:c.2863G>A | XP_016864752.1:p.Val955Met | |
| XM_017009264.2:c.2863G>A | XP_016864753.1:p.Val955Met | |
| XM_017009265.1:c.2863G>A | XP_016864754.1:p.Val955Met | |
| XM_017009266.1:c.2863G>A | XP_016864755.1:p.Val955Met | |
| XM_017009267.2:c.2863G>A | XP_016864756.1:p.Val955Met | |
| XM_017009268.1:c.2554G>A | XP_016864757.1:p.Val852Met | |
| XR_001742050.2:n.3097G>A | ||
| NM_182925.5:c.2632G>A MANE Select | NP_891555.2:p.Val878Met | |
| NM_001354989.2:c.2632G>A | NP_001341918.1:p.Val878Met | |
| NM_002020.5:c.2632G>A | NP_002011.2:p.Val878Met |