Canonical Allele Identifier: CA982865913
Gene:

Linked Data

dbSNP Id: rs1907316882

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237256G>T , CM000679.2:g.30237256G>T GRCh38
NC_000017.10:g.28564274G>T , CM000679.1:g.28564274G>T GRCh37
NC_000017.9:g.25588400G>T NCBI36
NG_011747.2:g.3681C>A

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.165+186G>T
XR_001752824.1:n.280+186G>T