Canonical Allele Identifier: CA462575196

Gene: TRHR

Linked Data

• gnomAD v4: 8-109087650-A-T
• MyVariant Identifiers: chr8:g.110099879A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.109087650A>T , CM000670.2:g.109087650A>T	GRCh38
NC_000008.10:g.110099879A>T , CM000670.1:g.110099879A>T	GRCh37
NC_000008.9:g.110169055A>T	NCBI36
NG_017161.1:g.5204A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000518632.2:c.138A>T MANE Select	ENSP00000430711.2:p.Val46=
ENST00000311762.2:c.138A>T	ENSP00000309818.2:p.Val46=
ENST00000518632.1:c.138A>T	ENSP00000430711.1:p.Val46=
NM_003301.5:c.138A>T	NP_003292.1:p.Val46=
XM_011517263.1:c.138A>T	XP_011515565.1:p.Val46=
XM_011517263.2:c.138A>T	XP_011515565.1:p.Val46=
NM_003301.7:c.138A>T MANE Select	NP_003292.1:p.Val46=