Canonical Allele Identifier: CA2652141735
Gene: THBD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23049557A>C , CM000682.2:g.23049557A>C GRCh38
NC_000020.10:g.23030194A>C , CM000682.1:g.23030194A>C GRCh37
NC_000020.9:g.22978194A>C NCBI36
NG_012027.1:g.5108T>G , LRG_168:g.5108T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.-53T>G MANE Select ENSP00000366307.2:n.-53T>G
ENST00000377103.2:c.-53T>G ENSP00000366307.2:n.-53T>G
NM_000361.2:c.-53T>G , LRG_168t1:c.-53T>G NP_000352.1:n.-53T>G
NM_000361.3:c.-53T>G MANE Select NP_000352.1:n.-53T>G