Canonical Allele Identifier: CA14661540

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41167943G>T , CM000681.2:g.41167943G>T	GRCh38
NC_000019.9:g.41673848G>T , CM000681.1:g.41673848G>T	GRCh37
NC_000019.8:g.46365688G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011527591.1:c.184+8016C>A	XP_011525893.1:n.184+8016C>A