Canonical Allele Identifier: CA775632396

Gene:

Linked Data

• dbSNP Id: rs1370948869
• MyVariant Identifiers: chr17:g.8041000G>A (hg19) ; chr17:g.8137682G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8137682G>A , CM000679.2:g.8137682G>A	GRCh38
NC_000017.10:g.8041000G>A , CM000679.1:g.8041000G>A	GRCh37
NC_000017.9:g.7981725G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_934202.1:n.183-1167G>A
XR_934203.1:n.70-1795G>A
XR_934202.2:n.414-1167G>A