Canonical Allele Identifier: CA2255111908
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237229A= , CM000679.2:g.30237229A= GRCh38
NC_000017.10:g.28564247A= , CM000679.1:g.28564247A= GRCh37
NC_000017.9:g.25588373A= NCBI36
NG_011747.2:g.3708T=

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+159A=
XR_001752824.1:n.280+159A=