Canonical Allele Identifier: CA183627956

Gene: TRHR

Linked Data

• dbSNP Id: rs1018104017
• MyVariant Identifiers: chr8:g.110109913A>T (hg19) ; chr8:g.109097684A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.109097684A>T , CM000670.2:g.109097684A>T	GRCh38
NC_000008.10:g.110109913A>T , CM000670.1:g.110109913A>T	GRCh37
NC_000008.9:g.110179089A>T	NCBI36
NG_017161.1:g.15238A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518632.2:c.789+9383A>T MANE Select	ENSP00000430711.2:n.789+9383A>T
ENST00000311762.2:c.789+9383A>T	ENSP00000309818.2:n.789+9383A>T
ENST00000518632.1:c.789+9383A>T	ENSP00000430711.1:n.789+9383A>T
NM_003301.5:c.789+9383A>T	NP_003292.1:n.789+9383A>T
XM_011517263.1:c.789+9383A>T	XP_011515565.1:n.789+9383A>T
XM_011517263.2:c.789+9383A>T	XP_011515565.1:n.789+9383A>T
NM_003301.7:c.789+9383A>T MANE Select	NP_003292.1:n.789+9383A>T