Canonical Allele Identifier: CA462575156

Gene: TRHR

Linked Data

• MyVariant Identifiers: chr8:g.110099822C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.109087593C>G , CM000670.2:g.109087593C>G	GRCh38
NC_000008.10:g.110099822C>G , CM000670.1:g.110099822C>G	GRCh37
NC_000008.9:g.110168998C>G	NCBI36
NG_017161.1:g.5147C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518632.2:c.81C>G MANE Select	ENSP00000430711.2:p.Val27=
ENST00000311762.2:c.81C>G	ENSP00000309818.2:p.Val27=
ENST00000518632.1:c.81C>G	ENSP00000430711.1:p.Val27=
NM_003301.5:c.81C>G	NP_003292.1:p.Val27=
XM_011517263.1:c.81C>G	XP_011515565.1:p.Val27=
XM_011517263.2:c.81C>G	XP_011515565.1:p.Val27=
NM_003301.7:c.81C>G MANE Select	NP_003292.1:p.Val27=