Canonical Allele Identifier: CA292625003

Gene:

Linked Data

• dbSNP Id: rs199693605
• MyVariant Identifiers: chr17:g.55866208C>A (hg19) ; chr17:g.57788847C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.57788847C>A , CM000679.2:g.57788847C>A	GRCh38
NC_000017.10:g.55866208C>A , CM000679.1:g.55866208C>A	GRCh37
NC_000017.9:g.53221207C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_934881.1:n.1608-16651G>T
XR_934881.3:n.3815-16651G>T