Canonical Allele Identifier:
CA1500739415
Gene:
Linked Data
dbSNP Id:
rs956482702
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.144601566A>T , CM000666.2:g.144601566A>T | GRCh38 |
| NC_000004.11:g.145522718A>T , CM000666.1:g.145522718A>T | GRCh37 |
| NC_000004.10:g.145742168A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649263.1:c.328-185588T>A | ENSP00000497507.1:n.328-185588T>A |