Canonical Allele Identifier: CA427349536
Gene:

Linked Data

gnomAD v3: 2-88016438-T-G
gnomAD v4: 2-88016438-T-G
MyVariant Identifiers: chr2:g.88315957T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016438T>G , CM000664.2:g.88016438T>G GRCh38
NC_000002.11:g.88315957T>G , CM000664.1:g.88315957T>G GRCh37
NC_000002.10:g.88097072T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.783T>G
XR_940336.3:n.783T>G
Search 100 bp 5'
Search 100 bp 3'