Canonical Allele Identifier:
CA464147389
Gene:
MyVariant.info:
GRCh37
chr9:g.21747803A>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.21747804A>T , CM000671.2:g.21747804A>T | GRCh38 |
| NC_000009.11:g.21747803A>T , CM000671.1:g.21747803A>T | GRCh37 |
| NC_000009.10:g.21737803A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001746563.2:n.163+20021T>A |