Canonical Allele Identifier: CA183627953
Gene: TRHR HGNC NCBI

Linked Data

dbSNP Id: rs1005706630
MyVariant Identifiers: chr8:g.109097656G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.109097656G>A , CM000670.2:g.109097656G>A GRCh38
NC_000008.10:g.110109885G>A , CM000670.1:g.110109885G>A GRCh37
NC_000008.9:g.110179061G>A NCBI36
NG_017161.1:g.15210G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000518632.2:c.789+9355G>A MANE Select ENSP00000430711.2:n.789+9355G>A
ENST00000311762.2:c.789+9355G>A ENSP00000309818.2:n.789+9355G>A
ENST00000518632.1:c.789+9355G>A ENSP00000430711.1:n.789+9355G>A
NM_003301.5:c.789+9355G>A NP_003292.1:n.789+9355G>A
XM_011517263.1:c.789+9355G>A XP_011515565.1:n.789+9355G>A
XM_011517263.2:c.789+9355G>A XP_011515565.1:n.789+9355G>A
NM_003301.7:c.789+9355G>A MANE Select NP_003292.1:n.789+9355G>A
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