Canonical Allele Identifier: CA2255112022
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237328T= , CM000679.2:g.30237328T= GRCh38
NC_000017.10:g.28564346T= , CM000679.1:g.28564346T= GRCh37
NC_000017.9:g.25588472T= NCBI36
NG_011747.2:g.3609A=

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.165+258T=
XR_001752824.1:n.280+258T=