Canonical Allele Identifier: CA2355680667
Gene: THBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23047714G= , CM000682.2:g.23047714G= GRCh38
NC_000020.10:g.23028351G= , CM000682.1:g.23028351G= GRCh37
NC_000020.9:g.22976351G= NCBI36
NG_012027.1:g.6951C= , LRG_168:g.6951C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.*63C= MANE Select ENSP00000366307.2:n.*63C=
ENST00000377103.2:c.*63C= ENSP00000366307.2:n.*63C=
NM_000361.2:c.*63C= , LRG_168t1:c.*63C= NP_000352.1:n.*63C=
NM_000361.3:c.*63C= MANE Select NP_000352.1:n.*63C=