Canonical Allele Identifier: CA2355680702
Gene: THBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23047766A= , CM000682.2:g.23047766A= GRCh38
NC_000020.10:g.23028403A= , CM000682.1:g.23028403A= GRCh37
NC_000020.9:g.22976403A= NCBI36
NG_012027.1:g.6899T= , LRG_168:g.6899T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.*11T= MANE Select ENSP00000366307.2:n.*11T=
ENST00000377103.2:c.*11T= ENSP00000366307.2:n.*11T=
NM_000361.2:c.*11T= , LRG_168t1:c.*11T= NP_000352.1:n.*11T=
NM_000361.3:c.*11T= MANE Select NP_000352.1:n.*11T=