Canonical Allele Identifier: CA185688688

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.126999634T>C , CM000670.2:g.126999634T>C	GRCh38
NC_000008.10:g.128011879T>C , CM000670.1:g.128011879T>C	GRCh37
NC_000008.9:g.128081061T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746076.2:n.1301-6921T>C