Canonical Allele Identifier: CA777817132

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24526812C>A , CM000680.2:g.24526812C>A	GRCh38
NC_000018.9:g.22106776C>A , CM000680.1:g.22106776C>A	GRCh37
NC_000018.8:g.20360774C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935294.1:n.1119-8724G>T