LDH info

Canonical Allele Identifier: CA308901790
Gene: CBLC HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3208856

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44793549C>G , CM000681.2:g.44793549C>G GRCh38
NC_000019.9:g.45296806C>G , CM000681.1:g.45296806C>G GRCh37
NC_000019.8:g.49988646C>G NCBI36
NG_054718.1:g.20695C>G

Transcript Alleles

HGVS Amino-acid change
NM_001130852.1:c.1075C>G VV NP_001124324.1:p.His359Asp
NM_012116.3:c.1213C>G VV NP_036248.3:p.His405Asp
XM_005258696.2:c.1213C>G XP_005258753.1:p.His405Asp
XM_011526688.1:c.1213C>G XP_011524990.1:p.His405Asp
XM_011526689.1:c.1075C>G XP_011524991.1:p.His359Asp
XR_935783.1:n.1160C>G
NM_012116.4:c.1213C>G VV MANE Preferred NP_036248.3:p.His405Asp
XM_005258696.3:c.1213C>G XP_005258753.1:p.His405Asp
XM_011526688.2:c.1213C>G XP_011524990.1:p.His405Asp
XM_011526689.2:c.1075C>G XP_011524991.1:p.His359Asp
XR_935783.2:n.1165C>G
ENST00000270279.7:c.1213C>G ENSP00000270279.3:p.His405Asp
ENST00000341505.4:c.1075C>G ENSP00000340250.4:p.His359Asp