Canonical Allele Identifier: CA15068083

Gene:

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161493708G>A , CM000663.2:g.161493708G>A	GRCh38
NC_000001.10:g.161463498G>A , CM000663.1:g.161463498G>A	GRCh37
NC_000001.9:g.159730122G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922214.1:n.2011+89G>A
XR_922214.2:n.2960+89G>A