Canonical Allele Identifier: CA894254099
Gene:

Linked Data

dbSNP Id: rs1481621783
MyVariant Identifiers: chr2:g.88315590G>C (hg19) chr2:g.88016071G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016071G>C , CM000664.2:g.88016071G>C GRCh38
NC_000002.11:g.88315590G>C , CM000664.1:g.88315590G>C GRCh37
NC_000002.10:g.88096705G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.416G>C
XR_940336.3:n.416G>C
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