Canonical Allele Identifier: CA10617925

Gene: THRB

Linked Data

• ClinVar Variation Id: 344544
• ClinVar RCV Id: RCV000342998
• dbSNP Id: rs886058267
• gnomAD v2: 3-24159253-T-G
• gnomAD v3: 3-24117762-T-G
• gnomAD v4: 3-24117762-T-G
• MyVariant Identifiers: chr3:g.24159253T>G (hg19) ; chr3:g.24117762T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.24117762T>G , CM000665.2:g.24117762T>G	GRCh38
NC_000003.11:g.24159253T>G , CM000665.1:g.24159253T>G	GRCh37
NC_000003.10:g.24134257T>G	NCBI36
NG_009159.1:g.382061A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396671.7:c.*5122A>C	ENSP00000379904.2:n.*5122A>C
ENST00000646209.2:c.*5122A>C MANE Select	ENSP00000496686.2:n.*5122A>C
ENST00000396671.6:c.*5122A>C	ENSP00000379904.2:n.*5122A>C
NM_000461.4:c.*5122A>C	NP_000452.2:n.*5122A>C
NM_001128176.2:c.*5122A>C	NP_001121648.1:n.*5122A>C
NM_001128177.1:c.*5122A>C	NP_001121649.1:n.*5122A>C
NM_001252634.1:c.*5122A>C	NP_001239563.1:n.*5122A>C
NM_001354708.1:c.*5122A>C	NP_001341637.1:n.*5122A>C
NM_001354709.1:c.*5122A>C	NP_001341638.1:n.*5122A>C
NM_001354710.1:c.*5122A>C	NP_001341639.1:n.*5122A>C
NM_001354711.1:c.*5122A>C	NP_001341640.1:n.*5122A>C
NM_001354712.1:c.*5122A>C	NP_001341641.1:n.*5122A>C
NM_001354713.1:c.*5122A>C	NP_001341642.1:n.*5122A>C
NM_001354714.1:c.*5122A>C	NP_001341643.1:n.*5122A>C
NM_001354715.1:c.*5122A>C	NP_001341644.1:n.*5122A>C
NM_000461.5:c.*5122A>C	NP_000452.2:n.*5122A>C
NM_001128176.3:c.*5122A>C	NP_001121648.1:n.*5122A>C
NM_001128177.2:c.*5122A>C	NP_001121649.1:n.*5122A>C
NM_001252634.2:c.*5122A>C	NP_001239563.1:n.*5122A>C
NM_001354708.2:c.*5122A>C	NP_001341637.1:n.*5122A>C
NM_001354709.2:c.*5122A>C	NP_001341638.1:n.*5122A>C
NM_001354710.2:c.*5122A>C	NP_001341639.1:n.*5122A>C
NM_001354711.2:c.*5122A>C	NP_001341640.1:n.*5122A>C
NM_001354712.2:c.*5122A>C MANE Select	NP_001341641.1:n.*5122A>C
NM_001354713.2:c.*5122A>C	NP_001341642.1:n.*5122A>C
NM_001354714.2:c.*5122A>C	NP_001341643.1:n.*5122A>C
NM_001354715.2:c.*5122A>C	NP_001341644.1:n.*5122A>C
NM_001374822.1:c.*5122A>C	NP_001361751.1:n.*5122A>C
NM_001374823.1:c.*5122A>C	NP_001361752.1:n.*5122A>C
NM_001374824.1:c.*5122A>C	NP_001361753.1:n.*5122A>C
NM_001374825.1:c.*5122A>C	NP_001361754.1:n.*5122A>C
NM_001374826.1:c.*5122A>C	NP_001361755.1:n.*5122A>C
NM_001374827.1:c.*5122A>C	NP_001361756.1:n.*5122A>C