LDH info

Canonical Allele Identifier: CA2178266

Identifiers and link-outs to other resources

ClinVar Variation Id: 440386
ClinVar RCV Id: RCV000507808
dbSNP Id: rs17868323

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233682324T>G , CM000664.2:g.233682324T>G GRCh38
NC_000002.11:g.234590970T>G , CM000664.1:g.234590970T>G GRCh37
NC_000002.10:g.234255709T>G NCBI36
NG_002601.2:g.97581T>G

Transcript Alleles

HGVS Amino-acid change
NM_019075.2:c.855+44947T>G (UGT1A10) VV NP_061948.1:p.=
NM_019076.4:c.855+63762T>G (UGT1A8) VV NP_061949.3:p.=
NM_019077.2:n.387T>G (UGT1A7) VV NP_061950.2:p.Asn129Lys
NM_021027.2:c.855+9535T>G (UGT1A9) VV NP_066307.1:p.=
NM_021027.3:c.855+9535T>G (UGT1A9) VV NP_066307.1:p.=
ENST00000344644.9:c.855+44947T>G ENSP00000343838.5:p.=
ENST00000354728.4:c.855+9535T>G ENSP00000346768.4:p.=
ENST00000373426.3:n.387T>G ENSP00000362525.3:p.Asn129Lys
ENST00000373445.1:c.855+44947T>G ENSP00000362544.1:p.=
ENST00000373450.4:c.855+63762T>G ENSP00000362549.4:p.=