Canonical Allele Identifier: CA1500739119
Gene:

Linked Data

dbSNP Id: rs1727413422

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601420G>A , CM000666.2:g.144601420G>A GRCh38
NC_000004.11:g.145522572G>A , CM000666.1:g.145522572G>A GRCh37
NC_000004.10:g.145742022G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-185442C>T ENSP00000497507.1:n.328-185442C>T