Canonical Allele Identifier: CA775632399

Gene:

Linked Data

• dbSNP Id: rs1484942317
• MyVariant Identifiers: chr17:g.8041021G>A (hg19) ; chr17:g.8137703G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8137703G>A , CM000679.2:g.8137703G>A	GRCh38
NC_000017.10:g.8041021G>A , CM000679.1:g.8041021G>A	GRCh37
NC_000017.9:g.7981746G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_934202.1:n.183-1146G>A
XR_934203.1:n.70-1774G>A
XR_934202.2:n.414-1146G>A