Canonical Allele Identifier: CA427349349
Gene:

Linked Data

dbSNP Id: rs1440199505
MyVariant Identifiers: chr2:g.88315875C>G (hg19) chr2:g.88016356C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016356C>G , CM000664.2:g.88016356C>G GRCh38
NC_000002.11:g.88315875C>G , CM000664.1:g.88315875C>G GRCh37
NC_000002.10:g.88096990C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.701C>G
XR_940336.3:n.701C>G
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