Canonical Allele Identifier: CA2625933657

Gene: TSHR

Linked Data

• ClinVar Variation Id: 2880057
• ClinVar RCV Id: RCV003713099
• gnomAD v4: 14-81142921-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81142921C>G , CM000676.2:g.81142921C>G	GRCh38
NC_000014.8:g.81609265C>G , CM000676.1:g.81609265C>G	GRCh37
NC_000014.7:g.80679018C>G	NCBI36
NG_009206.1:g.192397C>G , LRG_523:g.192397C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.882-19C>G MANE Select	ENSP00000298171.2:n.882-19C>G
ENST00000636454.1:n.800-19C>G
ENST00000298171.6:c.882-19C>G	ENSP00000298171.2:n.882-19C>G
ENST00000541158.6:c.882-19C>G	ENSP00000441235.2:n.882-19C>G
NM_000369.2:c.882-19C>G , LRG_523t1:c.882-19C>G	NP_000360.2:n.882-19C>G
XM_005268037.3:c.882-19C>G	XP_005268094.1:n.882-19C>G
XM_011537119.1:c.603-19C>G	XP_011535421.1:n.603-19C>G
XR_245790.3:n.2086+22272G>C
XR_429385.2:n.853+22272G>C
XR_429386.2:n.854+22272G>C
XR_944075.1:n.865+22272G>C
XR_944076.1:n.861+22272G>C
XR_944077.1:n.865+22272G>C
XR_944078.1:n.865+22272G>C
XR_944079.1:n.855+22272G>C
XM_005268037.4:c.882-19C>G	XP_005268094.1:n.882-19C>G
XM_011537119.2:c.603-19C>G	XP_011535421.1:n.603-19C>G
XR_001751021.1:n.2753+22272G>C
XR_001751022.1:n.2753+22272G>C
XR_001751023.1:n.2753+22272G>C
XR_944075.3:n.929+22272G>C
NM_000369.4:c.882-19C>G	NP_000360.2:n.882-19C>G
NM_000369.5:c.882-19C>G MANE Select	NP_000360.2:n.882-19C>G