Canonical Allele Identifier: CA427349392
Gene:

Linked Data

dbSNP Id: rs1373912558
MyVariant Identifiers: chr2:g.88315892G>A (hg19) chr2:g.88016373G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016373G>A , CM000664.2:g.88016373G>A GRCh38
NC_000002.11:g.88315892G>A , CM000664.1:g.88315892G>A GRCh37
NC_000002.10:g.88097007G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.718G>A
XR_940336.3:n.718G>A
Search 100 bp 5'
Search 100 bp 3'