Canonical Allele Identifier: CA287548669

Gene:

Linked Data

• dbSNP Id: rs745409326
• MyVariant Identifiers: chr17:g.8041105G>A (hg19) ; chr17:g.8137787G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8137787G>A , CM000679.2:g.8137787G>A	GRCh38
NC_000017.10:g.8041105G>A , CM000679.1:g.8041105G>A	GRCh37
NC_000017.9:g.7981830G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_934202.1:n.183-1062G>A
XR_934203.1:n.70-1690G>A
XR_934202.2:n.414-1062G>A