Canonical Allele Identifier: CA669444229
Gene: GRID1 HGNC NCBI

Linked Data

dbSNP Id: rs1193606572
gnomAD v3: 10-86337973-G-A
gnomAD v4: 10-86337973-G-A
MyVariant Identifiers: chr10:g.88097730G>A (hg19) chr10:g.86337973G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86337973G>A , CM000672.2:g.86337973G>A GRCh38
NC_000010.10:g.88097730G>A , CM000672.1:g.88097730G>A GRCh37
NC_000010.9:g.88087710G>A NCBI36
NG_011875.1:g.33521C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000327946.12:c.235+25968C>T MANE Select ENSP00000330148.7:n.235+25968C>T
ENST00000327946.11:c.235+25968C>T ENSP00000330148.7:n.235+25968C>T
ENST00000464741.2:c.235+25968C>T ENSP00000433064.1:n.235+25968C>T
NM_017551.2:c.235+25968C>T NP_060021.1:n.235+25968C>T
XM_011539720.1:c.235+25968C>T XP_011538022.1:n.235+25968C>T
XM_011539720.2:c.235+25968C>T XP_011538022.1:n.235+25968C>T
NM_017551.3:c.235+25968C>T MANE Select NP_060021.1:n.235+25968C>T
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