Canonical Allele Identifier: CA900829632

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.152112520A>C , CM000665.2:g.152112520A>C	GRCh38
NC_000003.11:g.151830309A>C , CM000665.1:g.151830309A>C	GRCh37
NC_000003.10:g.153312999A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_924587.1:n.533-38806T>G