Canonical Allele Identifier: CA7294346
Gene: TSHR HGNC NCBI

Linked Data

dbSNP Id: rs774488446

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.81142900G>A , CM000676.2:g.81142900G>A GRCh38
NC_000014.8:g.81609244G>A , CM000676.1:g.81609244G>A GRCh37
NC_000014.7:g.80678997G>A NCBI36
NG_009206.1:g.192376G>A , LRG_523:g.192376G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000298171.7:c.882-40G>A MANE Select ENSP00000298171.2:n.882-40G>A
ENST00000636454.1:n.800-40G>A
ENST00000298171.6:c.882-40G>A ENSP00000298171.2:n.882-40G>A
ENST00000541158.6:c.882-40G>A ENSP00000441235.2:n.882-40G>A
NM_000369.2:c.882-40G>A , LRG_523t1:c.882-40G>A NP_000360.2:n.882-40G>A
XM_005268037.3:c.882-40G>A XP_005268094.1:n.882-40G>A
XM_011537119.1:c.603-40G>A XP_011535421.1:n.603-40G>A
XR_245790.3:n.2086+22293C>T
XR_429385.2:n.853+22293C>T
XR_429386.2:n.854+22293C>T
XR_944075.1:n.865+22293C>T
XR_944076.1:n.861+22293C>T
XR_944077.1:n.865+22293C>T
XR_944078.1:n.865+22293C>T
XR_944079.1:n.855+22293C>T
XM_005268037.4:c.882-40G>A XP_005268094.1:n.882-40G>A
XM_011537119.2:c.603-40G>A XP_011535421.1:n.603-40G>A
XR_001751021.1:n.2753+22293C>T
XR_001751022.1:n.2753+22293C>T
XR_001751023.1:n.2753+22293C>T
XR_944075.3:n.929+22293C>T
NM_000369.4:c.882-40G>A NP_000360.2:n.882-40G>A
NM_000369.5:c.882-40G>A MANE Select NP_000360.2:n.882-40G>A