LDH info

Canonical Allele Identifier: CA14419312
Gene: NOS2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs944722

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27765011C>T , CM000679.2:g.27765011C>T GRCh38
NC_000017.10:g.26092037C>T , CM000679.1:g.26092037C>T GRCh37
NC_000017.9:g.23116164C>T NCBI36
NG_011470.1:g.40519G>A

Transcript Alleles

HGVS Amino-acid change
NM_000625.4:c.2428+524G>A VV MANE Preferred NP_000616.3:p.=
XM_011524859.1:c.2428+524G>A XP_011523161.1:p.=
XM_011524860.1:c.2425+524G>A XP_011523162.1:p.=
XM_011524861.1:c.2356+596G>A XP_011523163.1:p.=
XM_011524862.1:c.1762+524G>A XP_011523164.1:p.=
ENST00000313735.10:c.2428+524G>A ENSP00000327251.6:p.=
ENST00000621962.1:n.2311+524G>A ENSP00000482291.1:p.=