LDH info

Canonical Allele Identifier: CA14034718
Gene: TSHR HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2268458

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.80996551T>C , CM000676.2:g.80996551T>C GRCh38
NC_000014.8:g.81462895T>C , CM000676.1:g.81462895T>C GRCh37
NC_000014.7:g.80532648T>C NCBI36
NG_009206.1:g.46027T>C , LRG_523:g.46027T>C

Transcript Alleles

HGVS Amino-acid change
NM_000369.2:c.170+40701T>C , LRG_523t1:c.170+40701T>C NP_000360.2:p.=
NM_001018036.2:c.170+40701T>C VV NP_001018046.1:p.=
NM_001142626.2:c.170+40701T>C VV NP_001136098.1:p.=
XM_005268037.3:c.170+40701T>C XP_005268094.1:p.=
XM_005268039.1:c.170+40701T>C XP_005268096.1:p.=
XM_006720245.1:c.170+40701T>C XP_006720308.1:p.=
XM_011537119.1:c.-159+40701T>C XP_011535421.1:p.=
XM_005268037.4:c.170+40701T>C XP_005268094.1:p.=
XM_011537119.2:c.-159+40701T>C XP_011535421.1:p.=
ENST00000298171.6:c.170+40701T>C ENSP00000298171.2:p.=
ENST00000342443.10:c.170+40701T>C ENSP00000340113.6:p.=
ENST00000541158.6:c.170+40701T>C ENSP00000441235.2:p.=
ENST00000553763.1:n.270+40701T>C
ENST00000554263.5:c.170+40701T>C ENSP00000451202.1:p.=
ENST00000554435.1:c.170+40701T>C ENSP00000450549.1:p.=
ENST00000555326.5:c.170+40701T>C ENSP00000451092.1:p.=