Canonical Allele Identifier: CA669402977
Gene: GRID1 HGNC NCBI

Linked Data

dbSNP Id: rs1205632523
gnomAD v3: 10-85980936-T-C
gnomAD v4: 10-85980936-T-C
MyVariant Identifiers: chr10:g.87740693T>C (hg19) chr10:g.85980936T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.85980936T>C , CM000672.2:g.85980936T>C GRCh38
NC_000010.10:g.87740693T>C , CM000672.1:g.87740693T>C GRCh37
NC_000010.9:g.87730673T>C NCBI36
NG_011875.1:g.390558A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.727-64697A>G MANE Select ENSP00000330148.7:n.727-64697A>G
ENST00000327946.11:c.727-64697A>G ENSP00000330148.7:n.727-64697A>G
ENST00000464741.2:c.727-64697A>G ENSP00000433064.1:n.727-64697A>G
NM_017551.2:c.727-64697A>G NP_060021.1:n.727-64697A>G
XM_011539720.1:c.727-64697A>G XP_011538022.1:n.727-64697A>G
XM_011539720.2:c.727-64697A>G XP_011538022.1:n.727-64697A>G
NM_017551.3:c.727-64697A>G MANE Select NP_060021.1:n.727-64697A>G
Search 100 bp 5'
Search 100 bp 3'