Canonical Allele Identifier: CA122483
Gene: THRB HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 12551
ClinVar RCV Id: RCV000013378
dbSNP Id: rs121918692

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.24122943T>C , CM000665.2:g.24122943T>C GRCh38
NC_000003.10:g.24139438T>C NCBI36
NC_000003.11:g.24164434T>C , CM000665.1:g.24164434T>C GRCh37
NG_009159.1:g.376880A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000280696.9:c.1372A>G ENSP00000280696.5:p.Lys458Glu
ENST00000356447.8:c.1327A>G ENSP00000348827.4:p.Lys443Glu
ENST00000396671.6:c.1327A>G ENSP00000379904.2:p.Lys443Glu
ENST00000416420.5:c.1327A>G ENSP00000414444.1:p.Lys443Glu
NM_000461.4:c.1327A>G VV NP_000452.2:p.Lys443Glu
NM_001128176.2:c.1327A>G VV NP_001121648.1:p.Lys443Glu
NM_001128177.1:c.1327A>G VV NP_001121649.1:p.Lys443Glu
NM_001252634.1:c.1327A>G VV NP_001239563.1:p.Lys443Glu
XM_005265421.3:c.1327A>G XP_005265478.1:p.Lys443Glu
XM_005265423.3:c.1327A>G XP_005265480.1:p.Lys443Glu
XM_005265424.2:c.1327A>G XP_005265481.1:p.Lys443Glu
XM_006713317.2:c.1327A>G XP_006713380.1:p.Lys443Glu
XM_006713318.2:c.1327A>G XP_006713381.1:p.Lys443Glu
XM_011534046.1:c.1327A>G XP_011532348.1:p.Lys443Glu
XM_011534047.1:c.1327A>G XP_011532349.1:p.Lys443Glu
XM_011534048.1:c.1327A>G XP_011532350.1:p.Lys443Glu
XM_011534049.1:c.1327A>G XP_011532351.1:p.Lys443Glu
XM_011534050.1:c.1327A>G XP_011532352.1:p.Lys443Glu
XM_011534051.1:c.1327A>G XP_011532353.1:p.Lys443Glu
XM_011534052.1:c.1327A>G XP_011532354.1:p.Lys443Glu
XM_011534053.1:c.1234A>G XP_011532355.1:p.Lys412Glu
NM_001354708.1:c.1327A>G VV NP_001341637.1:p.Lys443Glu
NM_001354709.1:c.1327A>G VV NP_001341638.1:p.Lys443Glu
NM_001354710.1:c.1327A>G VV NP_001341639.1:p.Lys443Glu
NM_001354711.1:c.1327A>G VV NP_001341640.1:p.Lys443Glu
NM_001354712.1:c.1327A>G VV NP_001341641.1:p.Lys443Glu
NM_001354713.1:c.1327A>G VV NP_001341642.1:p.Lys443Glu
NM_001354714.1:c.1234A>G VV NP_001341643.1:p.Lys412Glu
NM_001354715.1:c.1234A>G VV NP_001341644.1:p.Lys412Glu
XM_006713318.3:c.1327A>G
XM_011534047.3:c.1327A>G
XM_011534050.2:c.1327A>G
XM_011534052.2:c.1327A>G
XM_011534053.2:c.1234A>G
XM_017007109.1:c.1327A>G XP_016862598.1:p.Lys443Glu
XM_017007111.1:c.1327A>G XP_016862600.1:p.Lys443Glu
XM_017007112.1:c.1327A>G XP_016862601.1:p.Lys443Glu
XM_017007113.1:c.1234A>G XP_016862602.1:p.Lys412Glu
XM_024453733.1:c.1327A>G XP_024309501.1:p.Lys443Glu
XM_024453734.1:c.1327A>G XP_024309502.1:p.Lys443Glu
XM_024453735.1:c.1327A>G XP_024309503.1:p.Lys443Glu
XM_024453736.1:c.1327A>G XP_024309504.1:p.Lys443Glu
XM_024453737.1:c.1327A>G XP_024309505.1:p.Lys443Glu
XM_024453738.1:c.1327A>G XP_024309506.1:p.Lys443Glu