Canonical Allele Identifier: CA51878236
Gene:

Linked Data

dbSNP Id: rs777675741
MyVariant Identifiers: chr2:g.88315426G>A (hg19) chr2:g.88015907G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88015907G>A , CM000664.2:g.88015907G>A GRCh38
NC_000002.11:g.88315426G>A , CM000664.1:g.88315426G>A GRCh37
NC_000002.10:g.88096541G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.252G>A
XR_940336.3:n.252G>A
Search 100 bp 5'
Search 100 bp 3'