Canonical Allele Identifier: CA1809870462

Gene: TRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.109097555C= , CM000670.2:g.109097555C=	GRCh38
NC_000008.10:g.110109784C= , CM000670.1:g.110109784C=	GRCh37
NC_000008.9:g.110178960C=	NCBI36
NG_017161.1:g.15109C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518632.2:c.789+9254C= MANE Select	ENSP00000430711.2:n.789+9254C=
ENST00000311762.2:c.789+9254C=	ENSP00000309818.2:n.789+9254C=
ENST00000518632.1:c.789+9254C=	ENSP00000430711.1:n.789+9254C=
NM_003301.5:c.789+9254C=	NP_003292.1:n.789+9254C=
XM_011517263.1:c.789+9254C=	XP_011515565.1:n.789+9254C=
XM_011517263.2:c.789+9254C=	XP_011515565.1:n.789+9254C=
NM_003301.7:c.789+9254C= MANE Select	NP_003292.1:n.789+9254C=