LDH info

Canonical Allele Identifier: CA34082325
Gene: PTGS2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4648262

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186679617C>A , CM000663.2:g.186679617C>A GRCh38
NC_000001.10:g.186648749C>A , CM000663.1:g.186648749C>A GRCh37
NC_000001.9:g.184915372C>A NCBI36
NG_028206.2:g.5811G>T

Transcript Alleles

HGVS Amino-acid change
NM_000963.3:c.53-179G>T VV NP_000954.1:p.=
NM_000963.4:c.53-179G>T VV MANE Preferred NP_000954.1:p.=
ENST00000367468.9:c.53-179G>T ENSP00000356438.5:p.=
ENST00000490885.6:n.186-179G>T
ENST00000559627.1:n.53-179G>T ENSP00000454130.1:p.=
ENST00000559800.1:n.186-179G>T