Canonical Allele Identifier: CA427349494
Gene:

Linked Data

gnomAD v3: 2-88016419-T-A
gnomAD v4: 2-88016419-T-A
MyVariant Identifiers: chr2:g.88315938T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016419T>A , CM000664.2:g.88016419T>A GRCh38
NC_000002.11:g.88315938T>A , CM000664.1:g.88315938T>A GRCh37
NC_000002.10:g.88097053T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.764T>A
XR_940336.3:n.764T>A