Canonical Allele Identifier: CA534638451
Gene:

Linked Data

dbSNP Id: rs1440754364
gnomAD v2: 2-88315867-A-G
gnomAD v3: 2-88016348-A-G
gnomAD v4: 2-88016348-A-G
MyVariant Identifiers: chr2:g.88315867A>G (hg19) chr2:g.88315867_88315871delinsGTGGT (hg19) chr2:g.88016348A>G (hg38) chr2:g.88016348_88016352delinsGTGGT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016348A>G , CM000664.2:g.88016348A>G GRCh38
NC_000002.11:g.88315867A>G , CM000664.1:g.88315867A>G GRCh37
NC_000002.10:g.88096982A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.693A>G
XR_940336.3:n.693A>G
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