Canonical Allele Identifier: CA1809864563

Gene: TRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.109087567G= , CM000670.2:g.109087567G=	GRCh38
NC_000008.10:g.110099796G= , CM000670.1:g.110099796G=	GRCh37
NC_000008.9:g.110168972G=	NCBI36
NG_017161.1:g.5121G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000518632.2:c.55G= MANE Select	ENSP00000430711.2:p.Val19=
ENST00000311762.2:c.55G=	ENSP00000309818.2:p.Val19=
ENST00000518632.1:c.55G=	ENSP00000430711.1:p.Val19=
NM_003301.5:c.55G=	NP_003292.1:p.Val19=
XM_011517263.1:c.55G=	XP_011515565.1:p.Val19=
XM_011517263.2:c.55G=	XP_011515565.1:p.Val19=
NM_003301.7:c.55G= MANE Select	NP_003292.1:p.Val19=