Canonical Allele Identifier: CA292897724

Gene:

Linked Data

• dbSNP Id: rs117985052
• MyVariant Identifiers: chr17:g.61583666G>A (hg19) ; chr17:g.63506305G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63506305G>A , CM000679.2:g.63506305G>A	GRCh38
NC_000017.10:g.61583666G>A , CM000679.1:g.61583666G>A	GRCh37
NC_000017.9:g.58937398G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577647.2:c.1970-751G>A	ENSP00000464149.1:n.1970-751G>A