LDH info

Canonical Allele Identifier: CA2178121

Identifiers and link-outs to other resources

dbSNP Id: rs58597806

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233672700G>A , CM000664.2:g.233672700G>A GRCh38
NC_000002.11:g.234581346G>A , CM000664.1:g.234581346G>A GRCh37
NC_000002.10:g.234246085G>A NCBI36
NG_002601.2:g.87957G>A

Transcript Alleles

HGVS Amino-acid change
NM_019075.2:c.855+35323G>A (UGT1A10) VV NP_061948.1:p.=
NM_019076.4:c.855+54138G>A (UGT1A8) VV NP_061949.3:p.=
NM_021027.2:c.766G>A (UGT1A9) VV NP_066307.1:p.Asp256Asn
NM_021027.3:c.766G>A (UGT1A9) VV NP_066307.1:p.Asp256Asn
ENST00000344644.9:c.855+35323G>A ENSP00000343838.5:p.=
ENST00000354728.4:c.766G>A ENSP00000346768.4:p.Asp256Asn
ENST00000373445.1:c.855+35323G>A ENSP00000362544.1:p.=
ENST00000373450.4:c.855+54138G>A ENSP00000362549.4:p.=