LDH info

Canonical Allele Identifier: CA14502628
Gene: NOS2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs16949

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27797673T>C , CM000679.2:g.27797673T>C GRCh38
NC_000017.10:g.26124699T>C , CM000679.1:g.26124699T>C GRCh37
NC_000017.9:g.23148826T>C NCBI36
NG_011470.1:g.7857A>G

Transcript Alleles

HGVS Amino-acid change
NM_000625.4:c.110+1027A>G VV MANE Preferred NP_000616.3:p.=
XM_011524859.1:c.110+1027A>G XP_011523161.1:p.=
XM_011524861.1:c.110+1027A>G XP_011523163.1:p.=
ENST00000313735.10:c.110+1027A>G ENSP00000327251.6:p.=
ENST00000621962.1:n.110+1027A>G ENSP00000482291.1:p.=