Canonical Allele Identifier: CA174148862

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23961174G>A , CM000670.2:g.23961174G>A	GRCh38
NC_000008.10:g.23818687G>A , CM000670.1:g.23818687G>A	GRCh37
NC_000008.9:g.23874632G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745844.1:n.138+42406G>A