Canonical Allele Identifier: CA2568657041

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.52722543C>A , CM000664.2:g.52722543C>A	GRCh38
NC_000002.11:g.52949681C>A , CM000664.1:g.52949681C>A	GRCh37
NC_000002.10:g.52803185C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_002959384.1:n.714G>T