Canonical Allele Identifier: CA2255111784
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237071G= , CM000679.2:g.30237071G= GRCh38
NC_000017.10:g.28564089G= , CM000679.1:g.28564089G= GRCh37
NC_000017.9:g.25588215G= NCBI36
NG_011747.2:g.3866C=

Transcript Alleles

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