Canonical Allele Identifier: CA408404980
Gene: THBD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23047799T>G , CM000682.2:g.23047799T>G GRCh38
NC_000020.10:g.23028436T>G , CM000682.1:g.23028436T>G GRCh37
NC_000020.9:g.22976436T>G NCBI36
NG_012027.1:g.6866A>C , LRG_168:g.6866A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000377103.3:c.1706A>C MANE Select ENSP00000366307.2:p.Glu569Ala
ENST00000377103.2:c.1706A>C ENSP00000366307.2:p.Glu569Ala
NM_000361.2:c.1706A>C , LRG_168t1:c.1706A>C NP_000352.1:p.Glu569Ala
NM_000361.3:c.1706A>C MANE Select NP_000352.1:p.Glu569Ala