Canonical Allele Identifier: CA462575205

Gene: TRHR

Linked Data

• MyVariant Identifiers: chr8:g.110099888T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.109087659T>G , CM000670.2:g.109087659T>G	GRCh38
NC_000008.10:g.110099888T>G , CM000670.1:g.110099888T>G	GRCh37
NC_000008.9:g.110169064T>G	NCBI36
NG_017161.1:g.5213T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518632.2:c.147T>G MANE Select	ENSP00000430711.2:p.Val49=
ENST00000311762.2:c.147T>G	ENSP00000309818.2:p.Val49=
ENST00000518632.1:c.147T>G	ENSP00000430711.1:p.Val49=
NM_003301.5:c.147T>G	NP_003292.1:p.Val49=
XM_011517263.1:c.147T>G	XP_011515565.1:p.Val49=
XM_011517263.2:c.147T>G	XP_011515565.1:p.Val49=
NM_003301.7:c.147T>G MANE Select	NP_003292.1:p.Val49=