Canonical Allele Identifier: CA427349530
Gene:

Linked Data

dbSNP Id: rs10169099
gnomAD v3: 2-88016435-C-G
gnomAD v4: 2-88016435-C-G
MyVariant Identifiers: chr2:g.88315954C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016435C>G , CM000664.2:g.88016435C>G GRCh38
NC_000002.11:g.88315954C>G , CM000664.1:g.88315954C>G GRCh37
NC_000002.10:g.88097069C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.780C>G
XR_940336.3:n.780C>G