LDH info

Canonical Allele Identifier: CA15675747
Gene: CYP2C8 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1341164

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.95041116T>C , CM000672.2:g.95041116T>C GRCh38
NC_000010.10:g.96800873T>C , CM000672.1:g.96800873T>C GRCh37
NC_000010.9:g.96790863T>C NCBI36
NG_007972.1:g.33382A>G

Transcript Alleles

HGVS Amino-acid change
NM_000770.3:c.1149+1774A>G VV MANE Preferred NP_000761.3:p.=
NM_001198853.1:c.939+1774A>G VV NP_001185782.1:p.=
NM_001198854.1:c.843+1774A>G VV NP_001185783.1:p.=
NM_001198855.1:c.939+1774A>G VV NP_001185784.1:p.=
XR_945610.1:n.1246-156A>G
ENST00000371270.5:c.1149+1774A>G ENSP00000360317.3:p.=
ENST00000479946.2:n.1454-156A>G
ENST00000490994.6:c.*935+1774A>G ENSP00000433314.1:p.=
ENST00000525991.5:c.*724+1774A>G ENSP00000433842.1:p.=
ENST00000526814.5:n.1404+1774A>G
ENST00000527420.5:c.1150-156A>G ENSP00000433191.1:p.=
ENST00000527953.5:n.1405-156A>G
ENST00000533320.5:n.1383+1774A>G
ENST00000535898.5:c.843+1774A>G ENSP00000445062.1:p.=
ENST00000539050.5:c.939+1774A>G ENSP00000442343.2:p.=
ENST00000623108.3:c.939+1774A>G ENSP00000485110.1:p.=
ENST00000628935.1:n.892-156A>G ENSP00000487145.1:p.=