Canonical Allele Identifier: CA2284239349
Gene:

Linked Data

dbSNP Id: rs1968768406
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321256C>A , CM000680.2:g.10321256C>A GRCh38
NC_000018.9:g.10321253C>A , CM000680.1:g.10321253C>A GRCh37
NC_000018.8:g.10311253C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+892G>T
XR_001753344.1:n.650+892G>T
XR_001753345.1:n.865G>T
XR_001753346.1:n.549+892G>T
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