Canonical Allele Identifier: CA427349510
Gene:

Linked Data

gnomAD v3: 2-88016426-C-A
gnomAD v4: 2-88016426-C-A
MyVariant Identifiers: chr2:g.88315945C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016426C>A , CM000664.2:g.88016426C>A GRCh38
NC_000002.11:g.88315945C>A , CM000664.1:g.88315945C>A GRCh37
NC_000002.10:g.88097060C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.771C>A
XR_940336.3:n.771C>A