Canonical Allele Identifier: CA51878370
Gene:

Linked Data

dbSNP Id: rs796935366
MyVariant Identifiers: chr2:g.88315871T>C (hg19) chr2:g.88016352T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016352T>C , CM000664.2:g.88016352T>C GRCh38
NC_000002.11:g.88315871T>C , CM000664.1:g.88315871T>C GRCh37
NC_000002.10:g.88096986T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.697T>C
XR_940336.3:n.697T>C
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