Canonical Allele Identifier: CA122503
Gene: THRB HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 12563
ClinVar RCV Id: RCV000013391
dbSNP Id: rs121918703

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.24122934A>G , CM000665.2:g.24122934A>G GRCh38
NC_000003.10:g.24139429A>G NCBI36
NC_000003.11:g.24164425A>G , CM000665.1:g.24164425A>G GRCh37
NG_009159.1:g.376889T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000280696.9:c.1381T>C ENSP00000280696.5:p.Cys461Arg
ENST00000356447.8:c.1336T>C ENSP00000348827.4:p.Cys446Arg
ENST00000396671.6:c.1336T>C ENSP00000379904.2:p.Cys446Arg
ENST00000416420.5:c.1336T>C ENSP00000414444.1:p.Cys446Arg
NM_000461.4:c.1336T>C VV NP_000452.2:p.Cys446Arg
NM_001128176.2:c.1336T>C VV NP_001121648.1:p.Cys446Arg
NM_001128177.1:c.1336T>C VV NP_001121649.1:p.Cys446Arg
NM_001252634.1:c.1336T>C VV NP_001239563.1:p.Cys446Arg
XM_005265421.3:c.1336T>C XP_005265478.1:p.Cys446Arg
XM_005265423.3:c.1336T>C XP_005265480.1:p.Cys446Arg
XM_005265424.2:c.1336T>C XP_005265481.1:p.Cys446Arg
XM_006713317.2:c.1336T>C XP_006713380.1:p.Cys446Arg
XM_006713318.2:c.1336T>C XP_006713381.1:p.Cys446Arg
XM_011534046.1:c.1336T>C XP_011532348.1:p.Cys446Arg
XM_011534047.1:c.1336T>C XP_011532349.1:p.Cys446Arg
XM_011534048.1:c.1336T>C XP_011532350.1:p.Cys446Arg
XM_011534049.1:c.1336T>C XP_011532351.1:p.Cys446Arg
XM_011534050.1:c.1336T>C XP_011532352.1:p.Cys446Arg
XM_011534051.1:c.1336T>C XP_011532353.1:p.Cys446Arg
XM_011534052.1:c.1336T>C XP_011532354.1:p.Cys446Arg
XM_011534053.1:c.1243T>C XP_011532355.1:p.Cys415Arg
NM_001354708.1:c.1336T>C VV NP_001341637.1:p.Cys446Arg
NM_001354709.1:c.1336T>C VV NP_001341638.1:p.Cys446Arg
NM_001354710.1:c.1336T>C VV NP_001341639.1:p.Cys446Arg
NM_001354711.1:c.1336T>C VV NP_001341640.1:p.Cys446Arg
NM_001354712.1:c.1336T>C VV NP_001341641.1:p.Cys446Arg
NM_001354713.1:c.1336T>C VV NP_001341642.1:p.Cys446Arg
NM_001354714.1:c.1243T>C VV NP_001341643.1:p.Cys415Arg
NM_001354715.1:c.1243T>C VV NP_001341644.1:p.Cys415Arg
XM_006713318.3:c.1336T>C
XM_011534047.3:c.1336T>C
XM_011534050.2:c.1336T>C
XM_011534052.2:c.1336T>C
XM_011534053.2:c.1243T>C
XM_017007109.1:c.1336T>C XP_016862598.1:p.Cys446Arg
XM_017007111.1:c.1336T>C XP_016862600.1:p.Cys446Arg
XM_017007112.1:c.1336T>C XP_016862601.1:p.Cys446Arg
XM_017007113.1:c.1243T>C XP_016862602.1:p.Cys415Arg
XM_024453733.1:c.1336T>C XP_024309501.1:p.Cys446Arg
XM_024453734.1:c.1336T>C XP_024309502.1:p.Cys446Arg
XM_024453735.1:c.1336T>C XP_024309503.1:p.Cys446Arg
XM_024453736.1:c.1336T>C XP_024309504.1:p.Cys446Arg
XM_024453737.1:c.1336T>C XP_024309505.1:p.Cys446Arg
XM_024453738.1:c.1336T>C XP_024309506.1:p.Cys446Arg