Canonical Allele Identifier: CA427349367

Gene:

Linked Data

• dbSNP Id: rs1672686362
• MyVariant Identifiers: chr2:g.88315882A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016363A>G , CM000664.2:g.88016363A>G	GRCh38
NC_000002.11:g.88315882A>G , CM000664.1:g.88315882A>G	GRCh37
NC_000002.10:g.88096997A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.708A>G
XR_940336.3:n.708A>G