Canonical Allele Identifier: CA2284239323
Gene:

Linked Data

dbSNP Id: rs1968767616
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321213G>T , CM000680.2:g.10321213G>T GRCh38
NC_000018.9:g.10321210G>T , CM000680.1:g.10321210G>T GRCh37
NC_000018.8:g.10311210G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+935C>A
XR_001753344.1:n.650+935C>A
XR_001753345.1:n.908C>A
XR_001753346.1:n.549+935C>A
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