Canonical Allele Identifier: CA1069062182
Gene:

Linked Data

dbSNP Id: rs1727416325

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601588C>A , CM000666.2:g.144601588C>A GRCh38
NC_000004.11:g.145522740C>A , CM000666.1:g.145522740C>A GRCh37
NC_000004.10:g.145742190C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-185610G>T ENSP00000497507.1:n.328-185610G>T