Canonical Allele Identifier: CA2763876276
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601455G>A , CM000666.2:g.144601455G>A GRCh38
NC_000004.11:g.145522607G>A , CM000666.1:g.145522607G>A GRCh37
NC_000004.10:g.145742057G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649263.1:c.328-185477C>T ENSP00000497507.1:n.328-185477C>T