Canonical Allele Identifier: CA191701690

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551292C>T , CM000671.2:g.25551292C>T	GRCh38
NC_000009.11:g.25551290C>T , CM000671.1:g.25551290C>T	GRCh37
NC_000009.10:g.25541290C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_929525.1:n.50-720G>A
XR_929525.2:n.674-720G>A