LDH info

Canonical Allele Identifier: CA126956
Gene: CYP2D6 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16893
dbSNP Id: rs1065852

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42130692G>A , CM000684.2:g.42130692G>A GRCh38
NC_000022.10:g.42526694G>A , CM000684.1:g.42526694G>A GRCh37
NC_000022.9:g.40856638G>A NCBI36
NG_008376.3:g.4300C>T
NG_008376.4:g.5119C>T

Transcript Alleles

HGVS Amino-acid change
NM_000106.5:c.100C>T VV NP_000097.3:p.Pro34Ser
NM_001025161.2:c.100C>T VV NP_001020332.2:p.Pro34Ser
XM_011529966.1:c.100C>T XP_011528268.1:p.Pro34Ser
XM_011529967.1:c.100C>T XP_011528269.1:p.Pro34Ser
XM_011529968.1:c.100C>T XP_011528270.1:p.Pro34Ser
XM_011529969.1:c.37+605C>T XP_011528271.1:p.=
XM_011529970.1:c.100C>T XP_011528272.1:p.Pro34Ser
XM_011529971.1:c.37+605C>T XP_011528273.1:p.=
XM_011529972.1:c.100C>T XP_011528274.1:p.Pro34Ser
XR_430455.2:n.328+4G>A
NM_000106.6:c.100C>T VV NP_000097.3:p.Pro34Ser
XR_002958749.1:n.275+4G>A
ENST00000359033.4:c.100C>T ENSP00000351927.4:p.Pro34Ser
ENST00000360608.9:c.100C>T ENSP00000353820.5:p.Pro34Ser
ENST00000389970.7:c.34C>T ENSP00000374620.4:p.Pro12Ser
ENST00000488442.1:n.122C>T