Canonical Allele Identifier: CA1364766897
Gene: TWF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52245578G= , CM000665.2:g.52245578G= GRCh38
NC_000003.11:g.52279594G= , CM000665.1:g.52279594G= GRCh37
NC_000003.10:g.52254634G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000679296.1:c.-270+1101C= ENSP00000504576.1:n.-270+1101C=