Canonical Allele Identifier: CA147948979

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131956291C>A , CM000668.2:g.131956291C>A	GRCh38
NC_000006.11:g.132277431C>A , CM000668.1:g.132277431C>A	GRCh37
NC_000006.10:g.132319124C>A	NCBI36
NG_016131.1:g.88G>T