Canonical Allele Identifier: CA2255111775
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237050C= , CM000679.2:g.30237050C= GRCh38
NC_000017.10:g.28564068C= , CM000679.1:g.28564068C= GRCh37
NC_000017.9:g.25588194C= NCBI36
NG_011747.2:g.3887G=

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.145C=
XR_001752824.1:n.260C=