Canonical Allele Identifier: CA427349466
Gene:

Linked Data

dbSNP Id: rs996022629
gnomAD v3: 2-88016403-A-T
gnomAD v4: 2-88016403-A-T
MyVariant Identifiers: chr2:g.88315922A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016403A>T , CM000664.2:g.88016403A>T GRCh38
NC_000002.11:g.88315922A>T , CM000664.1:g.88315922A>T GRCh37
NC_000002.10:g.88097037A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.748A>T
XR_940336.3:n.748A>T