LDH info

Canonical Allele Identifier: CA8454976
Gene: NOS2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3729508

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27782004T>C , CM000679.2:g.27782004T>C GRCh38
NC_000017.10:g.26109030T>C , CM000679.1:g.26109030T>C GRCh37
NC_000017.9:g.23133157T>C NCBI36
NG_011470.1:g.23526A>G

Transcript Alleles

HGVS Amino-acid change
NM_000625.4:c.722+11A>G VV MANE Preferred NP_000616.3:p.=
XM_011524859.1:c.722+11A>G XP_011523161.1:p.=
XM_011524860.1:c.719+11A>G XP_011523162.1:p.=
XM_011524861.1:c.722+11A>G XP_011523163.1:p.=
XM_011524862.1:c.56+11A>G XP_011523164.1:p.=
ENST00000313735.10:c.722+11A>G ENSP00000327251.6:p.=
ENST00000621962.1:n.722+11A>G ENSP00000482291.1:p.=