Canonical Allele Identifier: CA669444213
Gene: GRID1 HGNC NCBI

Linked Data

dbSNP Id: rs1365204421
gnomAD v3: 10-86337950-C-T
gnomAD v4: 10-86337950-C-T
MyVariant Identifiers: chr10:g.88097707C>T (hg19) chr10:g.86337950C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86337950C>T , CM000672.2:g.86337950C>T GRCh38
NC_000010.10:g.88097707C>T , CM000672.1:g.88097707C>T GRCh37
NC_000010.9:g.88087687C>T NCBI36
NG_011875.1:g.33544G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327946.12:c.235+25991G>A MANE Select ENSP00000330148.7:n.235+25991G>A
ENST00000327946.11:c.235+25991G>A ENSP00000330148.7:n.235+25991G>A
ENST00000464741.2:c.235+25991G>A ENSP00000433064.1:n.235+25991G>A
NM_017551.2:c.235+25991G>A NP_060021.1:n.235+25991G>A
XM_011539720.1:c.235+25991G>A XP_011538022.1:n.235+25991G>A
XM_011539720.2:c.235+25991G>A XP_011538022.1:n.235+25991G>A
NM_017551.3:c.235+25991G>A MANE Select NP_060021.1:n.235+25991G>A
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