LDH info

Canonical Allele Identifier: CA12676727
Gene: NOS3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2853792

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.151002789G>A , CM000669.2:g.151002789G>A GRCh38
NC_000007.13:g.150699877G>A , CM000669.1:g.150699877G>A GRCh37
NC_000007.12:g.150330810G>A NCBI36
NG_011992.1:g.16731G>A

Transcript Alleles

HGVS Amino-acid change
NM_000603.4:c.1752+485G>A VV NP_000594.2:p.=
NM_001160109.1:n.1752+485G>A VV NP_001153581.1:p.=
NM_001160110.1:n.1752+485G>A VV NP_001153582.1:p.=
NM_001160111.1:n.1753-362G>A VV NP_001153583.1:p.=
XM_006716002.2:c.1752+485G>A XP_006716065.1:p.=
NM_000603.5:c.1752+485G>A VV MANE Preferred NP_000594.2:p.=
ENST00000297494.7:c.1752+485G>A ENSP00000297494.3:p.=
ENST00000460603.1:n.205-47G>A
ENST00000461406.5:c.1134+485G>A ENSP00000417143.1:p.=
ENST00000467517.1:n.1752+485G>A ENSP00000420551.1:p.=
ENST00000484524.5:n.1753-362G>A ENSP00000420215.1:p.=