LDH info

Canonical Allele Identifier: CA337722119
Gene: DDX3Y HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs9341287

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12907213A>C , CM000686.2:g.12907213A>C GRCh38
NC_000024.9:g.15019124A>C , CM000686.1:g.15019124A>C GRCh37
NC_000024.8:g.13528518A>C NCBI36
NG_012831.1:g.8106A>C

Transcript Alleles

HGVS Amino-acid change
NM_001122665.2:c.46-324A>C VV NP_001116137.1:p.=
NM_001302552.1:c.37-324A>C VV NP_001289481.1:p.=
NM_004660.4:c.46-324A>C VV NP_004651.2:p.=
XM_006724878.1:c.46-324A>C XP_006724941.1:p.=
XM_011531471.1:c.46-324A>C XP_011529773.1:p.=
NM_001122665.3:c.46-324A>C VV NP_001116137.1:p.=
NM_001302552.2:c.37-324A>C VV NP_001289481.1:p.=
NM_001324195.1:c.46-324A>C VV NP_001311124.1:p.=
NR_136716.1:n.197-324A>C
NR_136717.1:n.197-324A>C
NR_136718.1:n.197-324A>C
NR_136719.1:n.197-324A>C
NR_136720.1:n.197-324A>C
NR_136721.1:n.125-324A>C
NR_136722.1:n.112-324A>C
NR_136723.1:n.112-324A>C
NR_136724.1:n.112-324A>C
XR_001756014.2:n.150-324A>C
NM_004660.5:c.46-324A>C VV MANE Preferred NP_004651.2:p.=
ENST00000336079.7:c.46-324A>C ENSP00000336725.3:p.=
ENST00000360160.8:c.46-324A>C ENSP00000353284.4:p.=
ENST00000440554.1:c.37-324A>C ENSP00000400377.1:p.=
ENST00000454054.5:c.46-324A>C ENSP00000398953.1:p.=
ENST00000493363.1:n.134-324A>C