Canonical Allele Identifier: CA51878237
Gene:

Linked Data

dbSNP Id: rs1047986692
MyVariant Identifiers: chr2:g.88315431C>T (hg19) chr2:g.88015912C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88015912C>T , CM000664.2:g.88015912C>T GRCh38
NC_000002.11:g.88315431C>T , CM000664.1:g.88315431C>T GRCh37
NC_000002.10:g.88096546C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.257C>T
XR_940336.3:n.257C>T
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Search 100 bp 3'