Canonical Allele Identifier: CA2255111774
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237045C= , CM000679.2:g.30237045C= GRCh38
NC_000017.10:g.28564063C= , CM000679.1:g.28564063C= GRCh37
NC_000017.9:g.25588189C= NCBI36
NG_011747.2:g.3892G=

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.140C=
XR_001752824.1:n.255C=