Canonical Allele Identifier: CA102057972
Gene: GRID2 HGNC NCBI

Linked Data

dbSNP Id: rs1051049155
MyVariant Identifiers: chr4:g.92775951G>A (hg38)
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Genomic Alleles

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

Transcript Alleles

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