Canonical Allele Identifier:
CA1500739176
Gene:
Linked Data
dbSNP Id:
rs1727413971
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.144601460G>A , CM000666.2:g.144601460G>A | GRCh38 |
| NC_000004.11:g.145522612G>A , CM000666.1:g.145522612G>A | GRCh37 |
| NC_000004.10:g.145742062G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649263.1:c.328-185482C>T | ENSP00000497507.1:n.328-185482C>T |