Canonical Allele Identifier: CA775632405

Gene:

Linked Data

• dbSNP Id: rs1249813238
• MyVariant Identifiers: chr17:g.8041056A>G (hg19) ; chr17:g.8137738A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8137738A>G , CM000679.2:g.8137738A>G	GRCh38
NC_000017.10:g.8041056A>G , CM000679.1:g.8041056A>G	GRCh37
NC_000017.9:g.7981781A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_934202.1:n.183-1111A>G
XR_934203.1:n.70-1739A>G
XR_934202.2:n.414-1111A>G