Canonical Allele Identifier: CA2255111816
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237140T= , CM000679.2:g.30237140T= GRCh38
NC_000017.10:g.28564158T= , CM000679.1:g.28564158T= GRCh37
NC_000017.9:g.25588284T= NCBI36
NG_011747.2:g.3797A=

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.165+70T=
XR_001752824.1:n.280+70T=