LDH info

Canonical Allele Identifier: CA122117

Identifiers and link-outs to other resources

ClinVar Variation Id: 12288
dbSNP Id: rs4124874

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233757013T>G , CM000664.2:g.233757013T>G GRCh38
NC_000002.11:g.234665659T>G , CM000664.1:g.234665659T>G GRCh37
NC_000002.10:g.234330398T>G NCBI36
NG_002601.2:g.172270T>G
NG_033238.1:g.1741T>G , LRG_733:g.1741T>G

Transcript Alleles

HGVS Amino-acid change
NM_001072.3:c.862-10021T>G (UGT1A6) VV NP_001063.2:p.=
NM_007120.2:c.868-10021T>G (UGT1A4) VV NP_009051.1:p.=
NM_019075.2:c.856-10021T>G (UGT1A10) VV NP_061948.1:p.=
NM_019076.4:c.856-10021T>G (UGT1A8) VV NP_061949.3:p.=
NM_019077.2:n.856-10021T>G (UGT1A7) VV NP_061950.2:p.=
NM_019078.1:n.868-10021T>G (UGT1A5) VV NP_061951.1:p.=
NM_019093.2:n.868-10021T>G (UGT1A3) VV NP_061966.1:p.=
NM_021027.2:c.856-10021T>G (UGT1A9) VV NP_066307.1:p.=
NM_205862.1:c.61-10021T>G (UGT1A6) VV NP_995584.1:p.=
NM_001072.4:c.862-10021T>G (UGT1A6) VV NP_001063.2:p.=
NM_021027.3:c.856-10021T>G (UGT1A9) VV NP_066307.1:p.=
NM_007120.3:c.868-10021T>G (UGT1A4) VV NP_009051.1:p.=
NM_019093.4:c.868-10021T>G (UGT1A3) VV NP_061966.1:p.=
NM_205862.2:c.61-10021T>G (UGT1A6) VV NP_995584.1:p.=
ENST00000305139.10:c.862-10021T>G ENSP00000303174.6:p.=
ENST00000344644.9:c.856-10021T>G ENSP00000343838.5:p.=
ENST00000354728.4:c.856-10021T>G ENSP00000346768.4:p.=
ENST00000373409.7:c.868-10021T>G ENSP00000362508.3:p.=
ENST00000373414.3:n.868-10021T>G ENSP00000362513.3:p.=
ENST00000373424.5:c.61-10021T>G ENSP00000362523.1:p.=
ENST00000373426.3:n.856-10021T>G ENSP00000362525.3:p.=
ENST00000373445.1:c.856-10021T>G ENSP00000362544.1:p.=
ENST00000373450.4:c.856-10021T>G ENSP00000362549.4:p.=
ENST00000406651.1:c.61-10021T>G ENSP00000386107.1:p.=
ENST00000446481.6:c.61-10021T>G ENSP00000401541.1:p.=
ENST00000450233.1:n.868-10021T>G ENSP00000408608.1:p.=
ENST00000482026.5:c.868-10021T>G ENSP00000418532.1:p.=
ENST00000484784.2:n.442-10021T>G ENSP00000419780.2:p.=