Canonical Allele Identifier: CA2255111776
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237051G= , CM000679.2:g.30237051G= GRCh38
NC_000017.10:g.28564069G= , CM000679.1:g.28564069G= GRCh37
NC_000017.9:g.25588195G= NCBI36
NG_011747.2:g.3886C=

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.146G=
XR_001752824.1:n.261G=