Canonical Allele Identifier: CA2332763298
Gene:

Linked Data

dbSNP Id: rs1971155173
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521991T>G , CM000681.2:g.33521991T>G GRCh38
NC_000019.9:g.34012897T>G , CM000681.1:g.34012897T>G GRCh37
NC_000019.8:g.38704737T>G NCBI36
NG_013358.1:g.4903A>C
NG_013358.2:g.4903A>C

Transcript Alleles

HGVS Amino-acid Change
XR_935918.1:n.50T>G
XR_935919.1:n.45T>G
XR_001754035.2:n.58T>G
XR_935918.2:n.58T>G
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