Canonical Allele Identifier: CA427349502
Gene:

Linked Data

gnomAD v3: 2-88016423-A-T
gnomAD v4: 2-88016423-A-T
MyVariant Identifiers: chr2:g.88315942A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016423A>T , CM000664.2:g.88016423A>T GRCh38
NC_000002.11:g.88315942A>T , CM000664.1:g.88315942A>T GRCh37
NC_000002.10:g.88097057A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.768A>T
XR_940336.3:n.768A>T