Canonical Allele Identifier: CA2284239351
Gene:

Linked Data

dbSNP Id: rs1968768441
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321257A>G , CM000680.2:g.10321257A>G GRCh38
NC_000018.9:g.10321254A>G , CM000680.1:g.10321254A>G GRCh37
NC_000018.8:g.10311254A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+891T>C
XR_001753344.1:n.650+891T>C
XR_001753345.1:n.864T>C
XR_001753346.1:n.549+891T>C
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