LDH info

Canonical Allele Identifier: CA7125298
Gene: PSME2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4575

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24146226T>C , CM000676.2:g.24146226T>C GRCh38
NC_000014.8:g.24615435T>C , CM000676.1:g.24615435T>C GRCh37
NC_000014.7:g.23685275T>C NCBI36
NG_042234.1:g.4352T>C

Transcript Alleles

HGVS Amino-acid change
NM_002818.2:c.63A>G VV NP_002809.2:p.Arg21=
XM_006720213.1:c.-293A>G XP_006720276.1:p.=
XM_006720213.2:c.-293A>G XP_006720276.1:p.=
NM_002818.3:c.63A>G VV MANE Preferred NP_002809.2:p.Arg21=
ENST00000216802.9:c.63A>G ENSP00000216802.5:p.Arg21=
ENST00000471700.6:n.61A>G
ENST00000558273.5:c.63A>G ENSP00000453195.1:p.Arg21=
ENST00000558931.5:n.740A>G
ENST00000559056.5:c.-169A>G ENSP00000452940.1:p.=
ENST00000559453.5:n.13A>G
ENST00000559493.5:n.60A>G
ENST00000559613.1:n.111A>G
ENST00000560370.3:c.63A>G ENSP00000453161.1:p.Arg21=
ENST00000560410.5:c.48+308A>G ENSP00000453487.1:p.=
ENST00000560592.5:n.103A>G
ENST00000560788.1:n.78A>G
ENST00000615264.4:c.63A>G ENSP00000484569.1:p.Arg21=
ENST00000630027.1:c.63A>G ENSP00000485798.1:p.Arg21=