Canonical Allele Identifier: CA1117758234
Gene: TRHR HGNC NCBI

Linked Data

dbSNP Id: rs1811613274
gnomAD v3: 8-109097569-G-C
gnomAD v4: 8-109097569-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.109097569G>C , CM000670.2:g.109097569G>C GRCh38
NC_000008.10:g.110109798G>C , CM000670.1:g.110109798G>C GRCh37
NC_000008.9:g.110178974G>C NCBI36
NG_017161.1:g.15123G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000518632.2:c.789+9268G>C MANE Select ENSP00000430711.2:n.789+9268G>C
ENST00000311762.2:c.789+9268G>C ENSP00000309818.2:n.789+9268G>C
ENST00000518632.1:c.789+9268G>C ENSP00000430711.1:n.789+9268G>C
NM_003301.5:c.789+9268G>C NP_003292.1:n.789+9268G>C
XM_011517263.1:c.789+9268G>C XP_011515565.1:n.789+9268G>C
XM_011517263.2:c.789+9268G>C XP_011515565.1:n.789+9268G>C
NM_003301.7:c.789+9268G>C MANE Select NP_003292.1:n.789+9268G>C
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