Canonical Allele Identifier: CA764892133

Gene:

Linked Data

• dbSNP Id: rs1296355517
• MyVariant Identifiers: chr2:g.219081305C>T (hg19) ; chr2:g.218216582C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218216582C>T , CM000664.2:g.218216582C>T	GRCh38
NC_000002.11:g.219081305C>T , CM000664.1:g.219081305C>T	GRCh37
NC_000002.10:g.218789550C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_241416.2:n.363G>A
XR_923908.1:n.360G>A