Canonical Allele Identifier: CA1809864562
Gene: TRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.109087566A= , CM000670.2:g.109087566A= GRCh38
NC_000008.10:g.110099795A= , CM000670.1:g.110099795A= GRCh37
NC_000008.9:g.110168971A= NCBI36
NG_017161.1:g.5120A=

Transcript Alleles

HGVS Amino-acid change
ENST00000518632.2:c.54A= MANE Select ENSP00000430711.2:p.Ala18=
ENST00000311762.2:c.54A= ENSP00000309818.2:p.Ala18=
ENST00000518632.1:c.54A= ENSP00000430711.1:p.Ala18=
NM_003301.5:c.54A= NP_003292.1:p.Ala18=
XM_011517263.1:c.54A= XP_011515565.1:p.Ala18=
XM_011517263.2:c.54A= XP_011515565.1:p.Ala18=
NM_003301.7:c.54A= MANE Select NP_003292.1:p.Ala18=