Canonical Allele Identifier: CA263934801

Gene: TSHR

Linked Data

• dbSNP Id: rs890141591
• gnomAD v4: 14-81142907-G-C
• MyVariant Identifiers: chr14:g.81609251G>C (hg19) ; chr14:g.81142907G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.81142907G>C , CM000676.2:g.81142907G>C	GRCh38
NC_000014.8:g.81609251G>C , CM000676.1:g.81609251G>C	GRCh37
NC_000014.7:g.80679004G>C	NCBI36
NG_009206.1:g.192383G>C , LRG_523:g.192383G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298171.7:c.882-33G>C MANE Select	ENSP00000298171.2:n.882-33G>C
ENST00000636454.1:n.800-33G>C
ENST00000298171.6:c.882-33G>C	ENSP00000298171.2:n.882-33G>C
ENST00000541158.6:c.882-33G>C	ENSP00000441235.2:n.882-33G>C
NM_000369.2:c.882-33G>C , LRG_523t1:c.882-33G>C	NP_000360.2:n.882-33G>C
XM_005268037.3:c.882-33G>C	XP_005268094.1:n.882-33G>C
XM_011537119.1:c.603-33G>C	XP_011535421.1:n.603-33G>C
XR_245790.3:n.2086+22286C>G
XR_429385.2:n.853+22286C>G
XR_429386.2:n.854+22286C>G
XR_944075.1:n.865+22286C>G
XR_944076.1:n.861+22286C>G
XR_944077.1:n.865+22286C>G
XR_944078.1:n.865+22286C>G
XR_944079.1:n.855+22286C>G
XM_005268037.4:c.882-33G>C	XP_005268094.1:n.882-33G>C
XM_011537119.2:c.603-33G>C	XP_011535421.1:n.603-33G>C
XR_001751021.1:n.2753+22286C>G
XR_001751022.1:n.2753+22286C>G
XR_001751023.1:n.2753+22286C>G
XR_944075.3:n.929+22286C>G
NM_000369.4:c.882-33G>C	NP_000360.2:n.882-33G>C
NM_000369.5:c.882-33G>C MANE Select	NP_000360.2:n.882-33G>C