Canonical Allele Identifier: CA775632419

Gene:

Linked Data

• dbSNP Id: rs1329499494
• MyVariant Identifiers: chr17:g.8041107A>G (hg19) ; chr17:g.8137789A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8137789A>G , CM000679.2:g.8137789A>G	GRCh38
NC_000017.10:g.8041107A>G , CM000679.1:g.8041107A>G	GRCh37
NC_000017.9:g.7981832A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_934202.1:n.183-1060A>G
XR_934203.1:n.70-1688A>G
XR_934202.2:n.414-1060A>G