Canonical Allele Identifier: CA982865876
Gene:

Linked Data

dbSNP Id: rs1907316338

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237251C>T , CM000679.2:g.30237251C>T GRCh38
NC_000017.10:g.28564269C>T , CM000679.1:g.28564269C>T GRCh37
NC_000017.9:g.25588395C>T NCBI36
NG_011747.2:g.3686G>A

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+181C>T
XR_001752824.1:n.280+181C>T