Canonical Allele Identifier: CA2255111848
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237165G= , CM000679.2:g.30237165G= GRCh38
NC_000017.10:g.28564183G= , CM000679.1:g.28564183G= GRCh37
NC_000017.9:g.25588309G= NCBI36
NG_011747.2:g.3772C=

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.165+95G=
XR_001752824.1:n.280+95G=