Canonical Allele Identifier: CA427349490
Gene:

Linked Data

dbSNP Id: rs1672689647
gnomAD v3: 2-88016417-A-G
gnomAD v4: 2-88016417-A-G
MyVariant Identifiers: chr2:g.88315936A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016417A>G , CM000664.2:g.88016417A>G GRCh38
NC_000002.11:g.88315936A>G , CM000664.1:g.88315936A>G GRCh37
NC_000002.10:g.88097051A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.762A>G
XR_940336.3:n.762A>G