Canonical Allele Identifier: CA51878371
Gene:

Linked Data

dbSNP Id: rs367574790
MyVariant Identifiers: chr2:g.88315872T>G (hg19) chr2:g.88016353T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016353T>G , CM000664.2:g.88016353T>G GRCh38
NC_000002.11:g.88315872T>G , CM000664.1:g.88315872T>G GRCh37
NC_000002.10:g.88096987T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.698T>G
XR_940336.3:n.698T>G
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