Canonical Allele Identifier: CA2332763294
Gene:

Linked Data

dbSNP Id: rs1600185034
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.33521989A>T , CM000681.2:g.33521989A>T GRCh38
NC_000019.9:g.34012895A>T , CM000681.1:g.34012895A>T GRCh37
NC_000019.8:g.38704735A>T NCBI36
NG_013358.1:g.4905T>A
NG_013358.2:g.4905T>A

Transcript Alleles

HGVS Amino-acid Change
XR_935918.1:n.48A>T
XR_935919.1:n.43A>T
XR_001754035.2:n.56A>T
XR_935918.2:n.56A>T
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