Canonical Allele Identifier: CA1809870482

Gene: TRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.109097569G= , CM000670.2:g.109097569G=	GRCh38
NC_000008.10:g.110109798G= , CM000670.1:g.110109798G=	GRCh37
NC_000008.9:g.110178974G=	NCBI36
NG_017161.1:g.15123G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518632.2:c.789+9268G= MANE Select	ENSP00000430711.2:n.789+9268G=
ENST00000311762.2:c.789+9268G=	ENSP00000309818.2:n.789+9268G=
ENST00000518632.1:c.789+9268G=	ENSP00000430711.1:n.789+9268G=
NM_003301.5:c.789+9268G=	NP_003292.1:n.789+9268G=
XM_011517263.1:c.789+9268G=	XP_011515565.1:n.789+9268G=
XM_011517263.2:c.789+9268G=	XP_011515565.1:n.789+9268G=
NM_003301.7:c.789+9268G= MANE Select	NP_003292.1:n.789+9268G=