Canonical Allele Identifier: CA2255111799
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237111G= , CM000679.2:g.30237111G= GRCh38
NC_000017.10:g.28564129G= , CM000679.1:g.28564129G= GRCh37
NC_000017.9:g.25588255G= NCBI36
NG_011747.2:g.3826C=

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.165+41G=
XR_001752824.1:n.280+41G=