Canonical Allele Identifier: CA2255111797
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237110T= , CM000679.2:g.30237110T= GRCh38
NC_000017.10:g.28564128T= , CM000679.1:g.28564128T= GRCh37
NC_000017.9:g.25588254T= NCBI36
NG_011747.2:g.3827A=

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+40T=
XR_001752824.1:n.280+40T=