LDH info

Canonical Allele Identifier: CA126943

Identifiers and link-outs to other resources

ClinVar Variation Id: 16879
ClinVar RCV Id: RCV000018375
dbSNP Id: rs72554627

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142912546A>G , CM000670.2:g.142912546A>G GRCh38
NC_000008.10:g.143993962A>G , CM000670.1:g.143993962A>G GRCh37
NC_000008.9:g.143990964A>G NCBI36
NG_008374.1:g.10298T>C

Transcript Alleles

HGVS Amino-acid change
NM_000498.3:c.1382T>C (CYP11B2) VV NP_000489.3:p.Leu461Pro
XM_011516877.1:c.1529T>C (CYP11B2) XP_011515179.1:p.Leu510Pro
XM_011516878.1:c.1460T>C (CYP11B2) XP_011515180.1:p.Leu487Pro
XM_011516879.1:c.1451T>C (CYP11B2) XP_011515181.1:p.Leu484Pro
XM_011516970.1:c.215-1417A>G (GML) XP_011515272.1:p.=
ENST00000323110.2:c.1382T>C ENSP00000325822.2:p.Leu461Pro
ENST00000522728.5:c.182-1417A>G ENSP00000430799.1:p.=