Canonical Allele Identifier: CA1373744092
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.70577255T= , CM000665.2:g.70577255T= GRCh38
NC_000003.11:g.70626406T= , CM000665.1:g.70626406T= GRCh37
NC_000003.10:g.70709096T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940947.1:n.406+1263A=
XR_001740559.1:n.366+1263A=