LDH info

Canonical Allele Identifier: CA337722269
Gene: DDX3Y HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs34812786

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12914721C>T , CM000686.2:g.12914721C>T GRCh38
NC_000024.9:g.15026633C>T , CM000686.1:g.15026633C>T GRCh37
NC_000024.8:g.13536027C>T NCBI36
NG_012831.1:g.15615C>T

Transcript Alleles

HGVS Amino-acid change
NM_001122665.2:c.759+72C>T VV NP_001116137.1:p.=
NM_001302552.1:c.750+72C>T VV NP_001289481.1:p.=
NM_004660.4:c.759+72C>T VV NP_004651.2:p.=
XM_006724878.1:c.759+72C>T XP_006724941.1:p.=
XM_011531471.1:c.759+72C>T XP_011529773.1:p.=
NM_001122665.3:c.759+72C>T VV NP_001116137.1:p.=
NM_001302552.2:c.750+72C>T VV NP_001289481.1:p.=
NM_001324195.1:c.759+72C>T VV NP_001311124.1:p.=
NR_136716.1:n.982C>T
NR_136717.1:n.990+72C>T
NR_136718.1:n.1062C>T
NR_136719.1:n.852C>T
NR_136720.1:n.982C>T
NR_136721.1:n.838+72C>T
NR_136722.1:n.905+72C>T
NR_136723.1:n.977C>T
NR_136724.1:n.897C>T
XR_001756014.2:n.863+72C>T
NM_004660.5:c.759+72C>T VV MANE Preferred NP_004651.2:p.=
ENST00000336079.7:c.759+72C>T ENSP00000336725.3:p.=
ENST00000360160.8:c.759+72C>T ENSP00000353284.4:p.=
ENST00000463199.1:n.277+72C>T
ENST00000472510.5:n.394C>T