Canonical Allele Identifier: CA51878233
Gene:

Linked Data

dbSNP Id: rs980492359
MyVariant Identifiers: chr2:g.88315392G>A (hg19) chr2:g.88015873G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88015873G>A , CM000664.2:g.88015873G>A GRCh38
NC_000002.11:g.88315392G>A , CM000664.1:g.88315392G>A GRCh37
NC_000002.10:g.88096507G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.218G>A
XR_940336.3:n.218G>A
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