LDH info

Canonical Allele Identifier: CA281982130
Gene: FTO HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12596210

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.53994059T>C , CM000678.2:g.53994059T>C GRCh38
NC_000016.9:g.54027971T>C , CM000678.1:g.54027971T>C GRCh37
NC_000016.8:g.52585472T>C NCBI36
NG_012969.1:g.295097T>C

Transcript Alleles

HGVS Amino-acid change
NM_001080432.2:c.1364+59950T>C VV NP_001073901.1:p.=
XM_011523313.1:c.1394+59950T>C XP_011521615.1:p.=
XM_011523316.1:c.1395-14369T>C XP_011521618.1:p.=
NM_001363891.1:c.1394+59950T>C VV NP_001350820.1:p.=
NM_001363894.1:c.1427+59950T>C VV NP_001350823.1:p.=
NM_001363896.1:c.1346+37270T>C VV NP_001350825.1:p.=
NM_001363897.1:c.1286+59950T>C VV NP_001350826.1:p.=
NM_001363898.1:c.1250+59950T>C VV NP_001350827.1:p.=
NM_001363899.1:c.1250+59950T>C VV NP_001350828.1:p.=
NM_001363900.1:c.1220+59950T>C VV NP_001350829.1:p.=
NM_001363901.1:c.1220+59950T>C VV NP_001350830.1:p.=
NM_001363903.1:c.1239+105108T>C VV NP_001350832.1:p.=
NM_001363905.1:c.851+59950T>C VV NP_001350834.1:p.=
NM_001363988.1:c.*22+37270T>C VV NP_001350917.1:p.=
NR_156761.1:n.614+59950T>C
XM_011523316.3:c.1395-14369T>C XP_011521618.1:p.=
XM_024450437.1:c.1365-14369T>C XP_024306205.1:p.=
NM_001080432.3:c.1364+59950T>C VV MANE Preferred NP_001073901.1:p.=
ENST00000268349.7:n.97+9105T>C ENSP00000268349.7:p.=
ENST00000431610.6:c.167+59950T>C ENSP00000415636.2:p.=
ENST00000460382.5:c.167+59950T>C ENSP00000417422.1:p.=
ENST00000463855.1:c.230+59950T>C ENSP00000417843.1:p.=
ENST00000464071.1:c.*523+59950T>C ENSP00000418424.1:p.=
ENST00000471389.5:c.1364+59950T>C ENSP00000418823.1:p.=