LDH info

Canonical Allele Identifier: CA14480967
Gene: NOS2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17722851

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.27783810T>A , CM000679.2:g.27783810T>A GRCh38
NC_000017.10:g.26110836T>A , CM000679.1:g.26110836T>A GRCh37
NC_000017.9:g.23134963T>A NCBI36
NG_011470.1:g.21720A>T

Transcript Alleles

HGVS Amino-acid change
NM_000625.4:c.468-704A>T VV MANE Preferred NP_000616.3:p.=
XM_011524859.1:c.468-704A>T XP_011523161.1:p.=
XM_011524860.1:c.465-704A>T XP_011523162.1:p.=
XM_011524861.1:c.468-704A>T XP_011523163.1:p.=
XM_011524862.1:c.-199-704A>T XP_011523164.1:p.=
ENST00000313735.10:c.468-704A>T ENSP00000327251.6:p.=
ENST00000621962.1:n.468-704A>T ENSP00000482291.1:p.=