Linked Data
ClinVar Variation Id:
42365
dbSNP Id:
rs397515812
gnomAD v2:
15-48760624-G-A
gnomAD v4:
15-48468427-G-A
COSMIC:
COSM962380
PubMed:
PMID:12068374
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48468427G>A , CM000677.2:g.48468427G>A | GRCh38 |
| NC_000015.9:g.48760624G>A , CM000677.1:g.48760624G>A | GRCh37 |
| NC_000015.8:g.46547916G>A | NCBI36 |
| NG_008805.2:g.182362C>T , LRG_778:g.182362C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.4567C>T | ENSP00000453958.2:p.Arg1523Ter | |
| ENST00000674301.2:c.4567C>T | ENSP00000501333.2:p.Arg1523Ter | |
| ENST00000684448.1:n.3241C>T | ||
| ENST00000316623.10:c.4567C>T MANE Select | ENSP00000325527.5:p.Arg1523Ter | |
| ENST00000316623.9:c.4567C>T | ENSP00000325527.5:p.Arg1523Ter | |
| ENST00000537463.6:c.*330C>T | ENSP00000440294.2:n.*330C>T | |
| NM_000138.4:c.4567C>T , LRG_778t1:c.4567C>T | NP_000129.3:p.Arg1523Ter | |
| NM_000138.5:c.4567C>T MANE Select | NP_000129.3:p.Arg1523Ter |