LDH info

Canonical Allele Identifier: CA13697228
Gene: NOS1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3782221

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117358076G>A , CM000674.2:g.117358076G>A GRCh38
NC_000012.11:g.117795881G>A , CM000674.1:g.117795881G>A GRCh37
NC_000012.10:g.116280264G>A NCBI36
NG_011991.2:g.8702C>T

Transcript Alleles

HGVS Amino-acid change
NM_000620.4:c.-421+3436C>T VV NP_000611.1:p.=
NM_001204218.1:c.-421+3436C>T VV NP_001191147.1:p.=
XM_011538398.1:c.-421+915C>T XP_011536700.1:p.=
NM_000620.5:c.-421+3436C>T VV MANE Preferred NP_000611.1:p.=
ENST00000317775.10:c.-421+3436C>T ENSP00000320758.6:p.=
ENST00000477584.1:n.118+3436C>T
ENST00000549189.1:n.471-26587C>T
ENST00000618760.4:c.-421+3436C>T ENSP00000477999.1:p.=