Canonical Allele Identifier: CA1373744052
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.70577219G= , CM000665.2:g.70577219G= GRCh38
NC_000003.11:g.70626370G= , CM000665.1:g.70626370G= GRCh37
NC_000003.10:g.70709060G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940947.1:n.407-1266C=
XR_001740559.1:n.367-1266C=