Canonical Allele Identifier: CA372040816
Gene: TRHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.109087583A>T , CM000670.2:g.109087583A>T GRCh38
NC_000008.10:g.110099812A>T , CM000670.1:g.110099812A>T GRCh37
NC_000008.9:g.110168988A>T NCBI36
NG_017161.1:g.5137A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000518632.2:c.71A>T MANE Select ENSP00000430711.2:p.Tyr24Phe
ENST00000311762.2:c.71A>T ENSP00000309818.2:p.Tyr24Phe
ENST00000518632.1:c.71A>T ENSP00000430711.1:p.Tyr24Phe
NM_003301.5:c.71A>T NP_003292.1:p.Tyr24Phe
XM_011517263.1:c.71A>T XP_011515565.1:p.Tyr24Phe
XM_011517263.2:c.71A>T XP_011515565.1:p.Tyr24Phe
NM_003301.7:c.71A>T MANE Select NP_003292.1:p.Tyr24Phe