Canonical Allele Identifier: CA4842762
Gene: TRHR HGNC NCBI

Linked Data

dbSNP Id: rs769794580
ExAC: 8:110099795 A / T
gnomAD v2: 8-110099795-A-T
MyVariant Identifiers: chr8:g.110099795A>T (hg19) chr8:g.109087566A>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000518632.2:c.54A>T MANE Select ENSP00000430711.2:p.Ala18=
ENST00000311762.2:c.54A>T ENSP00000309818.2:p.Ala18=
ENST00000518632.1:c.54A>T ENSP00000430711.1:p.Ala18=
NM_003301.5:c.54A>T NP_003292.1:p.Ala18=
XM_011517263.1:c.54A>T XP_011515565.1:p.Ala18=
XM_011517263.2:c.54A>T XP_011515565.1:p.Ala18=
NM_003301.7:c.54A>T MANE Select NP_003292.1:p.Ala18=
Search 100 bp 5'
Search 100 bp 3'