Canonical Allele Identifier:
CA2384216387
Gene:
Linked Data
dbSNP Id:
rs239713
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.27324157T>A , CM000683.2:g.27324157T>A | GRCh38 |
| NC_000021.8:g.28696476T>A , CM000683.1:g.28696476T>A | GRCh37 |
| NC_000021.7:g.27618347T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_430359.2:n.834+26342A>T | ||
| XR_937629.1:n.834+26342A>T | ||
| XR_937630.1:n.834+26342A>T | ||
| XR_430359.3:n.847+26342A>T | ||
| XR_937629.2:n.847+26342A>T |