Canonical Allele Identifier: CA51878269

Gene:

Linked Data

• dbSNP Id: rs755620798
• MyVariant Identifiers: chr2:g.88315620C>T (hg19) ; chr2:g.88016101C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016101C>T , CM000664.2:g.88016101C>T	GRCh38
NC_000002.11:g.88315620C>T , CM000664.1:g.88315620C>T	GRCh37
NC_000002.10:g.88096735C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.446C>T
XR_940336.3:n.446C>T