Canonical Allele Identifier: CA51878348
Gene:

Linked Data

dbSNP Id: rs916772163
gnomAD v3: 2-88016316-T-G
gnomAD v4: 2-88016316-T-G
MyVariant Identifiers: chr2:g.88016316T>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016316T>G , CM000664.2:g.88016316T>G GRCh38
NC_000002.11:g.88315835T>G , CM000664.1:g.88315835T>G GRCh37
NC_000002.10:g.88096950T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.661T>G
XR_940336.3:n.661T>G