Canonical Allele Identifier: CA756214913
Gene:

Linked Data

dbSNP Id: rs536528784
MyVariant Identifiers: chr2:g.123641472G>A (hg19) chr2:g.122883896G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883896G>A , CM000664.2:g.122883896G>A GRCh38
NC_000002.11:g.123641472G>A , CM000664.1:g.123641472G>A GRCh37
NC_000002.10:g.123357942G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-1046G>A
XR_001739692.1:n.1451-1046G>A
XR_923292.2:n.1358-1046G>A
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