Canonical Allele Identifier: CA1476836315
Gene: GRID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.92775944A= , CM000666.2:g.92775944A= GRCh38
NC_000004.11:g.93697095A= , CM000666.1:g.93697095A= GRCh37
NC_000004.10:g.93916118A= NCBI36
NG_034113.1:g.476546A=

Transcript Alleles

HGVS Amino-acid change
ENST00000282020.9:c.244+185658A= MANE Select ENSP00000282020.4:n.244+185658A=
ENST00000282020.8:c.244+185658A= ENSP00000282020.4:n.244+185658A=
ENST00000505687.5:n.416+185658A=
ENST00000510992.5:c.244+185658A= ENSP00000421257.1:n.244+185658A=
NM_001286838.1:c.244+185658A= NP_001273767.1:n.244+185658A=
NM_001510.3:c.244+185658A= NP_001501.2:n.244+185658A=
XM_017008122.2:c.244+185658A= XP_016863611.1:n.244+185658A=
XM_024454024.1:c.244+185658A= XP_024309792.1:n.244+185658A=
NM_001510.4:c.244+185658A= MANE Select NP_001501.2:n.244+185658A=