Canonical Allele Identifier: CA788849984

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148748354T>A , CM000666.2:g.148748354T>A	GRCh38
NC_000004.11:g.149669506T>A , CM000666.1:g.149669506T>A	GRCh37
NC_000004.10:g.149888956T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001741441.1:n.1746-118403T>A