Canonical Allele Identifier: CA210711663
Gene: GRID1 HGNC NCBI

Linked Data

dbSNP Id: rs564962659

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86337969A>C , CM000672.2:g.86337969A>C GRCh38
NC_000010.10:g.88097726A>C , CM000672.1:g.88097726A>C GRCh37
NC_000010.9:g.88087706A>C NCBI36
NG_011875.1:g.33525T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327946.12:c.235+25972T>G MANE Select ENSP00000330148.7:n.235+25972T>G
ENST00000327946.11:c.235+25972T>G ENSP00000330148.7:n.235+25972T>G
ENST00000464741.2:c.235+25972T>G ENSP00000433064.1:n.235+25972T>G
NM_017551.2:c.235+25972T>G NP_060021.1:n.235+25972T>G
XM_011539720.1:c.235+25972T>G XP_011538022.1:n.235+25972T>G
XM_011539720.2:c.235+25972T>G XP_011538022.1:n.235+25972T>G
NM_017551.3:c.235+25972T>G MANE Select NP_060021.1:n.235+25972T>G