Canonical Allele Identifier: CA800067187
Gene: GRID2 HGNC NCBI

Linked Data

dbSNP Id: rs1156573605
MyVariant Identifiers: chr4:g.93697073A>G (hg19) chr4:g.92775922A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.92775922A>G , CM000666.2:g.92775922A>G GRCh38
NC_000004.11:g.93697073A>G , CM000666.1:g.93697073A>G GRCh37
NC_000004.10:g.93916096A>G NCBI36
NG_034113.1:g.476524A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000282020.9:c.244+185636A>G MANE Select ENSP00000282020.4:n.244+185636A>G
ENST00000282020.8:c.244+185636A>G ENSP00000282020.4:n.244+185636A>G
ENST00000505687.5:n.416+185636A>G
ENST00000510992.5:c.244+185636A>G ENSP00000421257.1:n.244+185636A>G
NM_001286838.1:c.244+185636A>G NP_001273767.1:n.244+185636A>G
NM_001510.3:c.244+185636A>G NP_001501.2:n.244+185636A>G
XM_017008122.2:c.244+185636A>G XP_016863611.1:n.244+185636A>G
XM_024454024.1:c.244+185636A>G XP_024309792.1:n.244+185636A>G
NM_001510.4:c.244+185636A>G MANE Select NP_001501.2:n.244+185636A>G
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