LDH info

Canonical Allele Identifier: CA13768398
Gene: NOS1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs478597

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117313620G>A , CM000674.2:g.117313620G>A GRCh38
NC_000012.11:g.117751425G>A , CM000674.1:g.117751425G>A GRCh37
NC_000012.10:g.116235808G>A NCBI36
NG_011991.2:g.53158C>T

Transcript Alleles

HGVS Amino-acid change
NM_000620.4:c.726-2028C>T VV NP_000611.1:p.=
NM_001204218.1:c.726-2028C>T VV NP_001191147.1:p.=
XM_011538398.1:c.726-2028C>T XP_011536700.1:p.=
NM_000620.5:c.726-2028C>T VV MANE Preferred NP_000611.1:p.=
ENST00000317775.10:c.726-2028C>T ENSP00000320758.6:p.=
ENST00000338101.8:c.726-2028C>T ENSP00000337459.4:p.=
ENST00000344089.4:c.723-2028C>T ENSP00000339862.4:p.=
ENST00000618760.4:c.726-2028C>T ENSP00000477999.1:p.=