Canonical Allele Identifier: CA372040776

Gene: TRHR

Linked Data

• gnomAD v4: 8-109087564-G-T
• MyVariant Identifiers: chr8:g.110099793G>T (hg19) ; chr8:g.109087564G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.109087564G>T , CM000670.2:g.109087564G>T	GRCh38
NC_000008.10:g.110099793G>T , CM000670.1:g.110099793G>T	GRCh37
NC_000008.9:g.110168969G>T	NCBI36
NG_017161.1:g.5118G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000518632.2:c.52G>T MANE Select	ENSP00000430711.2:p.Ala18Ser
ENST00000311762.2:c.52G>T	ENSP00000309818.2:p.Ala18Ser
ENST00000518632.1:c.52G>T	ENSP00000430711.1:p.Ala18Ser
NM_003301.5:c.52G>T	NP_003292.1:p.Ala18Ser
XM_011517263.1:c.52G>T	XP_011515565.1:p.Ala18Ser
XM_011517263.2:c.52G>T	XP_011515565.1:p.Ala18Ser
NM_003301.7:c.52G>T MANE Select	NP_003292.1:p.Ala18Ser