Linked Data
ClinVar Variation Id:
431924
dbSNP Id:
rs363804
gnomAD v2:
15-48733968-C-T
gnomAD v3:
15-48441771-C-T
gnomAD v4:
15-48441771-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48441771C>T , CM000677.2:g.48441771C>T | GRCh38 |
| NC_000015.9:g.48733968C>T , CM000677.1:g.48733968C>T | GRCh37 |
| NC_000015.8:g.46521260C>T | NCBI36 |
| NG_008805.2:g.209018G>A , LRG_778:g.209018G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.6113G>A | ENSP00000453958.2:p.Cys2038Tyr | |
| ENST00000674301.2:c.6113G>A | ENSP00000501333.2:p.Cys2038Tyr | |
| ENST00000316623.10:c.6113G>A MANE Select | ENSP00000325527.5:p.Cys2038Tyr | |
| ENST00000674301.1:c.1112G>A | ENSP00000501333.1:p.Cys371Tyr | |
| ENST00000316623.9:c.6113G>A | ENSP00000325527.5:p.Cys2038Tyr | |
| ENST00000537463.6:c.*1876G>A | ENSP00000440294.2:n.*1876G>A | |
| ENST00000559133.5:c.1420G>A | ||
| ENST00000560820.1:n.233G>A | ||
| NM_000138.4:c.6113G>A , LRG_778t1:c.6113G>A | NP_000129.3:p.Cys2038Tyr | |
| NM_000138.5:c.6113G>A MANE Select | NP_000129.3:p.Cys2038Tyr |