Canonical Allele Identifier: CA1809864531
Gene: TRHR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.109087490C= , CM000670.2:g.109087490C= GRCh38
NC_000008.10:g.110099719C= , CM000670.1:g.110099719C= GRCh37
NC_000008.9:g.110168895C= NCBI36
NG_017161.1:g.5044C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000518632.2:c.-23C= MANE Select ENSP00000430711.2:n.-23C=
ENST00000311762.2:c.-23C= ENSP00000309818.2:n.-23C=
ENST00000518632.1:c.-23C= ENSP00000430711.1:n.-23C=
NM_003301.5:c.-23C= NP_003292.1:n.-23C=
XM_011517263.1:c.-23C= XP_011515565.1:n.-23C=
XM_011517263.2:c.-23C= XP_011515565.1:n.-23C=
NM_003301.7:c.-23C= MANE Select NP_003292.1:n.-23C=
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