Canonical Allele Identifier: CA894253979
Gene:

Linked Data

dbSNP Id: rs1446639701
MyVariant Identifiers: chr2:g.88315469T>C (hg19) chr2:g.88015950T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88015950T>C , CM000664.2:g.88015950T>C GRCh38
NC_000002.11:g.88315469T>C , CM000664.1:g.88315469T>C GRCh37
NC_000002.10:g.88096584T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.295T>C
XR_940336.3:n.295T>C
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