Canonical Allele Identifier: CA772782722

Gene:

Linked Data

• dbSNP Id: rs1464307389
• MyVariant Identifiers: chr17:g.48289174A>G (hg19) ; chr17:g.50211813A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50211813A>G , CM000679.2:g.50211813A>G	GRCh38
NC_000017.10:g.48289174A>G , CM000679.1:g.48289174A>G	GRCh37
NC_000017.9:g.45644173A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_934838.1:n.43-2022A>G