Linked Data
ClinVar Variation Id:
177940
ClinVar RCV Id:
RCV000154599
dbSNP Id:
rs727504411
COSMIC:
COSM5807823
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48487118G>T , CM000677.2:g.48487118G>T | GRCh38 |
| NC_000015.9:g.48779315G>T , CM000677.1:g.48779315G>T | GRCh37 |
| NC_000015.8:g.46566607G>T | NCBI36 |
| NG_008805.2:g.163671C>A , LRG_778:g.163671C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.3546C>A | ENSP00000453958.2:p.Cys1182Ter | |
| ENST00000674301.2:c.3546C>A | ENSP00000501333.2:p.Cys1182Ter | |
| ENST00000684448.1:n.2220C>A | ||
| ENST00000316623.10:c.3546C>A MANE Select | ENSP00000325527.5:p.Cys1182Ter | |
| ENST00000316623.9:c.3546C>A | ENSP00000325527.5:p.Cys1182Ter | |
| ENST00000537463.6:c.637-12468C>A | ENSP00000440294.2:n.637-12468C>A | |
| NM_000138.4:c.3546C>A , LRG_778t1:c.3546C>A | NP_000129.3:p.Cys1182Ter | |
| NM_000138.5:c.3546C>A MANE Select | NP_000129.3:p.Cys1182Ter |