Canonical Allele Identifier: CA2355680676
Gene: THBD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23047733G= , CM000682.2:g.23047733G= GRCh38
NC_000020.10:g.23028370G= , CM000682.1:g.23028370G= GRCh37
NC_000020.9:g.22976370G= NCBI36
NG_012027.1:g.6932C= , LRG_168:g.6932C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.*44C= MANE Select ENSP00000366307.2:n.*44C=
ENST00000377103.2:c.*44C= ENSP00000366307.2:n.*44C=
NM_000361.2:c.*44C= , LRG_168t1:c.*44C= NP_000352.1:n.*44C=
NM_000361.3:c.*44C= MANE Select NP_000352.1:n.*44C=