Canonical Allele Identifier: CA2255111836
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237159G= , CM000679.2:g.30237159G= GRCh38
NC_000017.10:g.28564177G= , CM000679.1:g.28564177G= GRCh37
NC_000017.9:g.25588303G= NCBI36
NG_011747.2:g.3778C=

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.165+89G=
XR_001752824.1:n.280+89G=