Canonical Allele Identifier: CA707762775

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.65291924G>C , CM000676.2:g.65291924G>C	GRCh38
NC_000014.8:g.65758642G>C , CM000676.1:g.65758642G>C	GRCh37
NC_000014.7:g.64828395G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943945.1:n.271+26567C>G