Canonical Allele Identifier: CA2284239312
Gene:

Linked Data

dbSNP Id: rs1968767152
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321196A>T , CM000680.2:g.10321196A>T GRCh38
NC_000018.9:g.10321193A>T , CM000680.1:g.10321193A>T GRCh37
NC_000018.8:g.10311193A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+952T>A
XR_001753344.1:n.650+952T>A
XR_001753345.1:n.925T>A
XR_001753346.1:n.549+952T>A
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