Canonical Allele Identifier: CA894254364
Gene:

Linked Data

dbSNP Id: rs182685926
MyVariant Identifiers: chr2:g.88315752G>C (hg19) chr2:g.88016233G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016233G>C , CM000664.2:g.88016233G>C GRCh38
NC_000002.11:g.88315752G>C , CM000664.1:g.88315752G>C GRCh37
NC_000002.10:g.88096867G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.578G>C
XR_940336.3:n.578G>C
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