LDH info

Canonical Allele Identifier: CA14327322
Gene: FTO HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10163409

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.54104968A>T , CM000678.2:g.54104968A>T GRCh38
NC_000016.9:g.54138880A>T , CM000678.1:g.54138880A>T GRCh37
NC_000016.8:g.52696381A>T NCBI36
NG_012969.1:g.406006A>T

Transcript Alleles

HGVS Amino-acid change
NM_001080432.2:c.1365-6794A>T VV NP_001073901.1:p.=
XM_011523313.1:c.1395-6794A>T XP_011521615.1:p.=
NM_001363891.1:c.1395-6794A>T VV NP_001350820.1:p.=
NM_001363894.1:c.1428-6794A>T VV NP_001350823.1:p.=
NM_001363896.1:c.1347-6794A>T VV NP_001350825.1:p.=
NM_001363897.1:c.1287-6794A>T VV NP_001350826.1:p.=
NM_001363898.1:c.1251-6794A>T VV NP_001350827.1:p.=
NM_001363899.1:c.1251-6794A>T VV NP_001350828.1:p.=
NM_001363900.1:c.1221-6794A>T VV NP_001350829.1:p.=
NM_001363901.1:c.1221-6794A>T VV NP_001350830.1:p.=
NM_001363903.1:c.1240-6794A>T VV NP_001350832.1:p.=
NM_001363905.1:c.852-6794A>T VV NP_001350834.1:p.=
NM_001363988.1:c.*23-6794A>T VV NP_001350917.1:p.=
NR_156761.1:n.615-6794A>T
NM_001080432.3:c.1365-6794A>T VV MANE Preferred NP_001073901.1:p.=
ENST00000268349.7:n.98-6794A>T ENSP00000268349.7:p.=
ENST00000431610.6:c.168-6794A>T ENSP00000415636.2:p.=
ENST00000460382.5:c.168-6794A>T ENSP00000417422.1:p.=
ENST00000463855.1:c.231-6794A>T ENSP00000417843.1:p.=
ENST00000464071.1:c.*524-6794A>T ENSP00000418424.1:p.=
ENST00000471389.5:c.1365-6794A>T ENSP00000418823.1:p.=
ENST00000472835.1:n.307-6794A>T