Canonical Allele Identifier: CA10615502
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 344535
ClinVar RCV Id: RCV000332070
dbSNP Id: rs886058266

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.24117453A>T , CM000665.2:g.24117453A>T GRCh38
NC_000003.11:g.24158944A>T , CM000665.1:g.24158944A>T GRCh37
NC_000003.10:g.24133948A>T NCBI36
NG_009159.1:g.382370T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000396671.7:c.*5431T>A ENSP00000379904.2:n.*5431T>A
ENST00000646209.2:c.*5431T>A MANE Select ENSP00000496686.2:n.*5431T>A
ENST00000396671.6:c.*5431T>A ENSP00000379904.2:n.*5431T>A
NM_000461.4:c.*5431T>A NP_000452.2:n.*5431T>A
NM_001128176.2:c.*5431T>A NP_001121648.1:n.*5431T>A
NM_001128177.1:c.*5431T>A NP_001121649.1:n.*5431T>A
NM_001252634.1:c.*5431T>A NP_001239563.1:n.*5431T>A
NM_001354708.1:c.*5431T>A NP_001341637.1:n.*5431T>A
NM_001354709.1:c.*5431T>A NP_001341638.1:n.*5431T>A
NM_001354710.1:c.*5431T>A NP_001341639.1:n.*5431T>A
NM_001354711.1:c.*5431T>A NP_001341640.1:n.*5431T>A
NM_001354712.1:c.*5431T>A NP_001341641.1:n.*5431T>A
NM_001354713.1:c.*5431T>A NP_001341642.1:n.*5431T>A
NM_001354714.1:c.*5431T>A NP_001341643.1:n.*5431T>A
NM_001354715.1:c.*5431T>A NP_001341644.1:n.*5431T>A
NM_000461.5:c.*5431T>A NP_000452.2:n.*5431T>A
NM_001128176.3:c.*5431T>A NP_001121648.1:n.*5431T>A
NM_001128177.2:c.*5431T>A NP_001121649.1:n.*5431T>A
NM_001252634.2:c.*5431T>A NP_001239563.1:n.*5431T>A
NM_001354708.2:c.*5431T>A NP_001341637.1:n.*5431T>A
NM_001354709.2:c.*5431T>A NP_001341638.1:n.*5431T>A
NM_001354710.2:c.*5431T>A NP_001341639.1:n.*5431T>A
NM_001354711.2:c.*5431T>A NP_001341640.1:n.*5431T>A
NM_001354712.2:c.*5431T>A MANE Select NP_001341641.1:n.*5431T>A
NM_001354713.2:c.*5431T>A NP_001341642.1:n.*5431T>A
NM_001354714.2:c.*5431T>A NP_001341643.1:n.*5431T>A
NM_001354715.2:c.*5431T>A NP_001341644.1:n.*5431T>A
NM_001374822.1:c.*5431T>A NP_001361751.1:n.*5431T>A
NM_001374823.1:c.*5431T>A NP_001361752.1:n.*5431T>A
NM_001374824.1:c.*5431T>A NP_001361753.1:n.*5431T>A
NM_001374825.1:c.*5431T>A NP_001361754.1:n.*5431T>A
NM_001374826.1:c.*5431T>A NP_001361755.1:n.*5431T>A
NM_001374827.1:c.*5431T>A NP_001361756.1:n.*5431T>A