Canonical Allele Identifier: CA289219280

Gene:

Linked Data

• dbSNP Id: rs892770736
• MyVariant Identifiers: chr17:g.27703295C>T (hg19) ; chr17:g.29376277C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.29376277C>T , CM000679.2:g.29376277C>T	GRCh38
NC_000017.10:g.27703295C>T , CM000679.1:g.27703295C>T	GRCh37
NC_000017.9:g.24727421C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011525588.1:c.1008-5972G>A	XP_011523890.1:n.1008-5972G>A