Canonical Allele Identifier: CA372040788
Gene: TRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.110099800T>A (hg19) chr8:g.109087571T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.109087571T>A , CM000670.2:g.109087571T>A GRCh38
NC_000008.10:g.110099800T>A , CM000670.1:g.110099800T>A GRCh37
NC_000008.9:g.110168976T>A NCBI36
NG_017161.1:g.5125T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000518632.2:c.59T>A MANE Select ENSP00000430711.2:p.Val20Glu
ENST00000311762.2:c.59T>A ENSP00000309818.2:p.Val20Glu
ENST00000518632.1:c.59T>A ENSP00000430711.1:p.Val20Glu
NM_003301.5:c.59T>A NP_003292.1:p.Val20Glu
XM_011517263.1:c.59T>A XP_011515565.1:p.Val20Glu
XM_011517263.2:c.59T>A XP_011515565.1:p.Val20Glu
NM_003301.7:c.59T>A MANE Select NP_003292.1:p.Val20Glu
Search 100 bp 5'
Search 100 bp 3'