Canonical Allele Identifier: CA2564916961

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31439645C>A , CM000668.2:g.31439645C>A	GRCh38
NC_000006.11:g.31407422C>A , CM000668.1:g.31407422C>A	GRCh37
NC_000006.10:g.31515401C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_926694.1:n.462G>T