Canonical Allele Identifier: CA2739713809
Gene: THBD HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23049570A>T , CM000682.2:g.23049570A>T GRCh38
NC_000020.10:g.23030207A>T , CM000682.1:g.23030207A>T GRCh37
NC_000020.9:g.22978207A>T NCBI36
NG_012027.1:g.5095T>A , LRG_168:g.5095T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.-66T>A MANE Select ENSP00000366307.2:n.-66T>A
ENST00000377103.2:c.-66T>A ENSP00000366307.2:n.-66T>A
NM_000361.2:c.-66T>A , LRG_168t1:c.-66T>A NP_000352.1:n.-66T>A
NM_000361.3:c.-66T>A MANE Select NP_000352.1:n.-66T>A
Search 100 bp 5'
Search 100 bp 3'