Canonical Allele Identifier: CA701268533

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.80065389T>A , CM000675.2:g.80065389T>A	GRCh38
NC_000013.10:g.80639524T>A , CM000675.1:g.80639524T>A	GRCh37
NC_000013.9:g.79537525T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011535340.1:c.370+4390A>T	XP_011533642.1:n.370+4390A>T