Canonical Allele Identifier: CA1476836317
Gene: GRID2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.92775947A= , CM000666.2:g.92775947A= GRCh38
NC_000004.11:g.93697098A= , CM000666.1:g.93697098A= GRCh37
NC_000004.10:g.93916121A= NCBI36
NG_034113.1:g.476549A=

Transcript Alleles

HGVS Amino-acid change
ENST00000282020.9:c.244+185661A= MANE Select ENSP00000282020.4:n.244+185661A=
ENST00000282020.8:c.244+185661A= ENSP00000282020.4:n.244+185661A=
ENST00000505687.5:n.416+185661A=
ENST00000510992.5:c.244+185661A= ENSP00000421257.1:n.244+185661A=
NM_001286838.1:c.244+185661A= NP_001273767.1:n.244+185661A=
NM_001510.3:c.244+185661A= NP_001501.2:n.244+185661A=
XM_017008122.2:c.244+185661A= XP_016863611.1:n.244+185661A=
XM_024454024.1:c.244+185661A= XP_024309792.1:n.244+185661A=
NM_001510.4:c.244+185661A= MANE Select NP_001501.2:n.244+185661A=