Canonical Allele Identifier: CA372040720

Gene: TRHR

Linked Data

• COSMIC: COSM4149491
• MyVariant Identifiers: chr8:g.110099766C>G (hg19) ; chr8:g.109087537C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.109087537C>G , CM000670.2:g.109087537C>G	GRCh38
NC_000008.10:g.110099766C>G , CM000670.1:g.110099766C>G	GRCh37
NC_000008.9:g.110168942C>G	NCBI36
NG_017161.1:g.5091C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518632.2:c.25C>G MANE Select	ENSP00000430711.2:p.Leu9Val
ENST00000311762.2:c.25C>G	ENSP00000309818.2:p.Leu9Val
ENST00000518632.1:c.25C>G	ENSP00000430711.1:p.Leu9Val
NM_003301.5:c.25C>G	NP_003292.1:p.Leu9Val
XM_011517263.1:c.25C>G	XP_011515565.1:p.Leu9Val
XM_011517263.2:c.25C>G	XP_011515565.1:p.Leu9Val
NM_003301.7:c.25C>G MANE Select	NP_003292.1:p.Leu9Val