Canonical Allele Identifier: CA372040760
Gene: TRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.110099785A>C (hg19) chr8:g.109087556A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.109087556A>C , CM000670.2:g.109087556A>C GRCh38
NC_000008.10:g.110099785A>C , CM000670.1:g.110099785A>C GRCh37
NC_000008.9:g.110168961A>C NCBI36
NG_017161.1:g.5110A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000518632.2:c.44A>C MANE Select ENSP00000430711.2:p.Gln15Pro
ENST00000311762.2:c.44A>C ENSP00000309818.2:p.Gln15Pro
ENST00000518632.1:c.44A>C ENSP00000430711.1:p.Gln15Pro
NM_003301.5:c.44A>C NP_003292.1:p.Gln15Pro
XM_011517263.1:c.44A>C XP_011515565.1:p.Gln15Pro
XM_011517263.2:c.44A>C XP_011515565.1:p.Gln15Pro
NM_003301.7:c.44A>C MANE Select NP_003292.1:p.Gln15Pro
Search 100 bp 5'
Search 100 bp 3'