Canonical Allele Identifier: CA292625002

Gene:

Linked Data

• dbSNP Id: rs977087790
• MyVariant Identifiers: chr17:g.55866189G>A (hg19) ; chr17:g.57788828G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.57788828G>A , CM000679.2:g.57788828G>A	GRCh38
NC_000017.10:g.55866189G>A , CM000679.1:g.55866189G>A	GRCh37
NC_000017.9:g.53221188G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_934881.1:n.1608-16632C>T
XR_934881.3:n.3815-16632C>T