Canonical Allele Identifier: CA1476836320
Gene: GRID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.92775951G= , CM000666.2:g.92775951G= GRCh38
NC_000004.11:g.93697102G= , CM000666.1:g.93697102G= GRCh37
NC_000004.10:g.93916125G= NCBI36
NG_034113.1:g.476553G=

Transcript Alleles

HGVS Amino-acid change
ENST00000282020.9:c.244+185665G= MANE Select ENSP00000282020.4:n.244+185665G=
ENST00000282020.8:c.244+185665G= ENSP00000282020.4:n.244+185665G=
ENST00000505687.5:n.416+185665G=
ENST00000510992.5:c.244+185665G= ENSP00000421257.1:n.244+185665G=
NM_001286838.1:c.244+185665G= NP_001273767.1:n.244+185665G=
NM_001510.3:c.244+185665G= NP_001501.2:n.244+185665G=
XM_017008122.2:c.244+185665G= XP_016863611.1:n.244+185665G=
XM_024454024.1:c.244+185665G= XP_024309792.1:n.244+185665G=
NM_001510.4:c.244+185665G= MANE Select NP_001501.2:n.244+185665G=