Canonical Allele Identifier: CA462575154

Gene: TRHR

Linked Data

• MyVariant Identifiers: chr8:g.110099819G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.109087590G>C , CM000670.2:g.109087590G>C	GRCh38
NC_000008.10:g.110099819G>C , CM000670.1:g.110099819G>C	GRCh37
NC_000008.9:g.110168995G>C	NCBI36
NG_017161.1:g.5144G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518632.2:c.78G>C MANE Select	ENSP00000430711.2:p.Val26=
ENST00000311762.2:c.78G>C	ENSP00000309818.2:p.Val26=
ENST00000518632.1:c.78G>C	ENSP00000430711.1:p.Val26=
NM_003301.5:c.78G>C	NP_003292.1:p.Val26=
XM_011517263.1:c.78G>C	XP_011515565.1:p.Val26=
XM_011517263.2:c.78G>C	XP_011515565.1:p.Val26=
NM_003301.7:c.78G>C MANE Select	NP_003292.1:p.Val26=