Canonical Allele Identifier: CA2255112078
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237411T= , CM000679.2:g.30237411T= GRCh38
NC_000017.10:g.28564429T= , CM000679.1:g.28564429T= GRCh37
NC_000017.9:g.25588555T= NCBI36
NG_011747.2:g.3526A=

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.166-231T=
XR_001752824.1:n.281-231T=