Canonical Allele Identifier: CA1809870587
Gene: TRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.109097687C= , CM000670.2:g.109097687C= GRCh38
NC_000008.10:g.110109916C= , CM000670.1:g.110109916C= GRCh37
NC_000008.9:g.110179092C= NCBI36
NG_017161.1:g.15241C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000518632.2:c.789+9386C= MANE Select ENSP00000430711.2:n.789+9386C=
ENST00000311762.2:c.789+9386C= ENSP00000309818.2:n.789+9386C=
ENST00000518632.1:c.789+9386C= ENSP00000430711.1:n.789+9386C=
NM_003301.5:c.789+9386C= NP_003292.1:n.789+9386C=
XM_011517263.1:c.789+9386C= XP_011515565.1:n.789+9386C=
XM_011517263.2:c.789+9386C= XP_011515565.1:n.789+9386C=
NM_003301.7:c.789+9386C= MANE Select NP_003292.1:n.789+9386C=