Canonical Allele Identifier: CA1329878873

Gene:

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.220855368G>T , CM000664.2:g.220855368G>T	GRCh38
NC_000002.11:g.221720088G>T , CM000664.1:g.221720088G>T	GRCh37
NC_000002.10:g.221428332G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001739895.1:n.321-1686C>A
XR_001739896.1:n.321-1686C>A
XR_001739897.1:n.305-1686C>A
XR_001739902.1:n.276-367G>T