Canonical Allele Identifier: CA13996439
Gene: TSHR HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs179247

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.80966202A>G , CM000676.2:g.80966202A>G GRCh38
NC_000014.8:g.81432546A>G , CM000676.1:g.81432546A>G GRCh37
NC_000014.7:g.80502299A>G NCBI36
NG_009206.1:g.15678A>G , LRG_523:g.15678A>G

Transcript Alleles

HGVS Amino-acid change
NM_000369.2:c.170+10352A>G , LRG_523t1:c.170+10352A>G NP_000360.2:p.=
NM_001018036.2:c.170+10352A>G VV NP_001018046.1:p.=
NM_001142626.2:c.170+10352A>G VV NP_001136098.1:p.=
XM_005268037.3:c.170+10352A>G XP_005268094.1:p.=
XM_005268039.1:c.170+10352A>G XP_005268096.1:p.=
XM_006720245.1:c.170+10352A>G XP_006720308.1:p.=
XM_011537119.1:c.-159+10352A>G XP_011535421.1:p.=
XM_005268037.4:c.170+10352A>G XP_005268094.1:p.=
XM_011537119.2:c.-159+10352A>G XP_011535421.1:p.=
ENST00000298171.6:c.170+10352A>G ENSP00000298171.2:p.=
ENST00000342443.10:c.170+10352A>G ENSP00000340113.6:p.=
ENST00000541158.6:c.170+10352A>G ENSP00000441235.2:p.=
ENST00000553763.1:n.270+10352A>G
ENST00000554263.5:c.170+10352A>G ENSP00000451202.1:p.=
ENST00000554435.1:c.170+10352A>G ENSP00000450549.1:p.=
ENST00000555326.5:c.170+10352A>G ENSP00000451092.1:p.=