LDH info

Canonical Allele Identifier: CA2178317

Identifiers and link-outs to other resources

ClinVar Variation Id: 440389
ClinVar RCV Id: RCV000507753
dbSNP Id: rs11692021

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233682559T>C , CM000664.2:g.233682559T>C GRCh38
NC_000002.11:g.234591205T>C , CM000664.1:g.234591205T>C GRCh37
NC_000002.10:g.234255944T>C NCBI36
NG_002601.2:g.97816T>C

Transcript Alleles

HGVS Amino-acid change
NM_019075.2:c.855+45182T>C (UGT1A10) VV NP_061948.1:p.=
NM_019076.4:c.855+63997T>C (UGT1A8) VV NP_061949.3:p.=
NM_019077.2:n.622T>C (UGT1A7) VV NP_061950.2:p.Trp208Arg
NM_021027.2:c.855+9770T>C (UGT1A9) VV NP_066307.1:p.=
NM_021027.3:c.855+9770T>C (UGT1A9) VV NP_066307.1:p.=
ENST00000344644.9:c.855+45182T>C ENSP00000343838.5:p.=
ENST00000354728.4:c.855+9770T>C ENSP00000346768.4:p.=
ENST00000373426.3:n.622T>C ENSP00000362525.3:p.Trp208Arg
ENST00000373445.1:c.855+45182T>C ENSP00000362544.1:p.=
ENST00000373450.4:c.855+63997T>C ENSP00000362549.4:p.=
ENST00000485022.1:n.192T>C