Canonical Allele Identifier: CA2206404169

Gene:

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9249490G>T , CM000678.2:g.9249490G>T	GRCh38
NC_000016.9:g.9343347G>T , CM000678.1:g.9343347G>T	GRCh37
NC_000016.8:g.9250848G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_933054.1:n.70+64757G>T