Canonical Allele Identifier: CA427349411

Gene:

Linked Data

• dbSNP Id: rs1672686981
• MyVariant Identifiers: chr2:g.88315898C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016379C>T , CM000664.2:g.88016379C>T	GRCh38
NC_000002.11:g.88315898C>T , CM000664.1:g.88315898C>T	GRCh37
NC_000002.10:g.88097013C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.724C>T
XR_940336.3:n.724C>T