LDH info

Canonical Allele Identifier: CA213660

Identifiers and link-outs to other resources

ClinVar Variation Id: 1179
dbSNP Id: rs104894069

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142879690G>A , CM000670.2:g.142879690G>A GRCh38
NC_000008.10:g.143961106G>A , CM000670.1:g.143961106G>A GRCh37
NC_000008.9:g.143958108G>A NCBI36
NG_007954.1:g.5131C>T

Transcript Alleles

HGVS Amino-acid change
NM_000497.3:c.124C>T (CYP11B1) VV NP_000488.3:p.Pro42Ser
NM_001026213.1:c.124C>T (CYP11B1) VV NP_001021384.1:p.Pro42Ser
XM_011516870.1:c.124C>T (CYP11B1) XP_011515172.1:p.Pro42Ser
XM_011516871.1:c.124C>T (CYP11B1) XP_011515173.1:p.Pro42Ser
XM_011516872.1:c.124C>T (CYP11B1) XP_011515174.1:p.Pro42Ser
XM_011516873.1:c.124C>T (CYP11B1) XP_011515175.1:p.Pro42Ser
XM_011516874.1:c.124C>T (CYP11B1) XP_011515176.1:p.Pro42Ser
XM_011516876.1:c.124C>T (CYP11B1) XP_011515178.1:p.Pro42Ser
XM_011516970.1:c.215-34273G>A (GML) XP_011515272.1:p.=
ENST00000292427.8:c.124C>T ENSP00000292427.4:p.Pro42Ser
ENST00000314111.4:n.157C>T
ENST00000377675.3:c.124C>T ENSP00000366903.3:p.Pro42Ser
ENST00000517471.5:c.124C>T ENSP00000428043.1:p.Pro42Ser
ENST00000522728.5:c.182-34273G>A ENSP00000430799.1:p.=