Canonical Allele Identifier: CA845420152

Gene: TRHR

Linked Data

• dbSNP Id: rs1191502557
• MyVariant Identifiers: chr8:g.110109791G>A (hg19) ; chr8:g.109097562G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.109097562G>A , CM000670.2:g.109097562G>A	GRCh38
NC_000008.10:g.110109791G>A , CM000670.1:g.110109791G>A	GRCh37
NC_000008.9:g.110178967G>A	NCBI36
NG_017161.1:g.15116G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518632.2:c.789+9261G>A MANE Select	ENSP00000430711.2:n.789+9261G>A
ENST00000311762.2:c.789+9261G>A	ENSP00000309818.2:n.789+9261G>A
ENST00000518632.1:c.789+9261G>A	ENSP00000430711.1:n.789+9261G>A
NM_003301.5:c.789+9261G>A	NP_003292.1:n.789+9261G>A
XM_011517263.1:c.789+9261G>A	XP_011515565.1:n.789+9261G>A
XM_011517263.2:c.789+9261G>A	XP_011515565.1:n.789+9261G>A
NM_003301.7:c.789+9261G>A MANE Select	NP_003292.1:n.789+9261G>A