Canonical Allele Identifier: CA1117758260
Gene: TRHR HGNC NCBI

Linked Data

dbSNP Id: rs1342964613
gnomAD v3: 8-109097690-G-A
gnomAD v4: 8-109097690-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.109097690G>A , CM000670.2:g.109097690G>A GRCh38
NC_000008.10:g.110109919G>A , CM000670.1:g.110109919G>A GRCh37
NC_000008.9:g.110179095G>A NCBI36
NG_017161.1:g.15244G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000518632.2:c.789+9389G>A MANE Select ENSP00000430711.2:n.789+9389G>A
ENST00000311762.2:c.789+9389G>A ENSP00000309818.2:n.789+9389G>A
ENST00000518632.1:c.789+9389G>A ENSP00000430711.1:n.789+9389G>A
NM_003301.5:c.789+9389G>A NP_003292.1:n.789+9389G>A
XM_011517263.1:c.789+9389G>A XP_011515565.1:n.789+9389G>A
XM_011517263.2:c.789+9389G>A XP_011515565.1:n.789+9389G>A
NM_003301.7:c.789+9389G>A MANE Select NP_003292.1:n.789+9389G>A
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