Canonical Allele Identifier: CA2255111785
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237073G= , CM000679.2:g.30237073G= GRCh38
NC_000017.10:g.28564091G= , CM000679.1:g.28564091G= GRCh37
NC_000017.9:g.25588217G= NCBI36
NG_011747.2:g.3864C=

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.165+3G=
XR_001752824.1:n.280+3G=