Canonical Allele Identifier: CA727804458

Gene:

Linked Data

• dbSNP Id: rs2138852
• MyVariant Identifiers: chr17:g.27703349C>G (hg19) ; chr17:g.29376331C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.29376331C>G , CM000679.2:g.29376331C>G	GRCh38
NC_000017.10:g.27703349C>G , CM000679.1:g.27703349C>G	GRCh37
NC_000017.9:g.24727475C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011525588.1:c.1008-6026G>C	XP_011523890.1:n.1008-6026G>C