Canonical Allele Identifier: CA427349413

Gene:

Linked Data

• dbSNP Id: rs1418463953
• MyVariant Identifiers: chr2:g.88315899T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016380T>C , CM000664.2:g.88016380T>C	GRCh38
NC_000002.11:g.88315899T>C , CM000664.1:g.88315899T>C	GRCh37
NC_000002.10:g.88097014T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.725T>C
XR_940336.3:n.725T>C