Canonical Allele Identifier: CA2255111819
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237143A= , CM000679.2:g.30237143A= GRCh38
NC_000017.10:g.28564161A= , CM000679.1:g.28564161A= GRCh37
NC_000017.9:g.25588287A= NCBI36
NG_011747.2:g.3794T=

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.165+73A=
XR_001752824.1:n.280+73A=