Canonical Allele Identifier: CA372040751

Gene: TRHR

Linked Data

• MyVariant Identifiers: chr8:g.110099780G>T (hg19) ; chr8:g.109087551G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.109087551G>T , CM000670.2:g.109087551G>T	GRCh38
NC_000008.10:g.110099780G>T , CM000670.1:g.110099780G>T	GRCh37
NC_000008.9:g.110168956G>T	NCBI36
NG_017161.1:g.5105G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518632.2:c.39G>T MANE Select	ENSP00000430711.2:p.Gln13His
ENST00000311762.2:c.39G>T	ENSP00000309818.2:p.Gln13His
ENST00000518632.1:c.39G>T	ENSP00000430711.1:p.Gln13His
NM_003301.5:c.39G>T	NP_003292.1:p.Gln13His
XM_011517263.1:c.39G>T	XP_011515565.1:p.Gln13His
XM_011517263.2:c.39G>T	XP_011515565.1:p.Gln13His
NM_003301.7:c.39G>T MANE Select	NP_003292.1:p.Gln13His