LDH info

Canonical Allele Identifier: CA11756203
Gene: GRID2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1030757

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.92776002C>A , CM000666.2:g.92776002C>A GRCh38
NC_000004.11:g.93697153C>A , CM000666.1:g.93697153C>A GRCh37
NC_000004.10:g.93916176C>A NCBI36
NG_034113.1:g.476604C>A

Transcript Alleles

HGVS Amino-acid change
NM_001286838.1:c.244+185716C>A VV NP_001273767.1:p.=
NM_001510.3:c.244+185716C>A VV NP_001501.2:p.=
XM_017008122.2:c.244+185716C>A XP_016863611.1:p.=
XM_024454024.1:c.244+185716C>A XP_024309792.1:p.=
NM_001510.4:c.244+185716C>A VV MANE Preferred NP_001501.2:p.=
ENST00000282020.8:c.244+185716C>A ENSP00000282020.4:p.=
ENST00000505687.5:n.416+185716C>A
ENST00000510992.5:n.244+185716C>A ENSP00000421257.1:p.=