Linked Data
ClinVar Variation Id:
462873
dbSNP Id:
rs141806715
ExAC:
9:6550885 G / A
gnomAD v2:
9-6550885-G-A
gnomAD v3:
9-6550885-G-A
gnomAD v4:
9-6550885-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.6550885G>A , CM000671.2:g.6550885G>A | GRCh38 |
| NC_000009.11:g.6550885G>A , CM000671.1:g.6550885G>A | GRCh37 |
| NC_000009.10:g.6540885G>A | NCBI36 |
| NG_016397.1:g.99808C>T , LRG_643:g.99808C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000321612.8:c.2487C>T MANE Select | ENSP00000370737.4:p.Ala829= | |
| ENST00000638233.1:n.922C>T | ||
| ENST00000638661.1:c.687C>T | ENSP00000491369.1:p.Ala229= | |
| ENST00000638694.1:n.674C>T | ||
| ENST00000639318.1:c.687C>T | ENSP00000491932.1:p.Ala229= | |
| ENST00000639364.1:n.2187C>T | ||
| ENST00000639443.1:n.2055C>T | ||
| ENST00000639639.1:c.189C>T | ENSP00000491312.1:p.Ala63= | |
| ENST00000639954.1:n.2195C>T | ||
| ENST00000640505.1:n.726C>T | ||
| ENST00000321612.6:c.2487C>T | ENSP00000370737.3:p.Ala829= | |
| NM_000170.2:c.2487C>T , LRG_643t1:c.2487C>T | NP_000161.2:p.Ala829= | |
| NM_000170.3:c.2487C>T MANE Select | NP_000161.2:p.Ala829= |