Canonical Allele Identifier: CA1723318384
Gene: GRM3 HGNC NCBI

Linked Data

dbSNP Id: rs1798006091

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815935A>T , CM000669.2:g.86815935A>T GRCh38
NC_000007.13:g.86445251A>T , CM000669.1:g.86445251A>T GRCh37
NC_000007.12:g.86283187A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-22904A>T MANE Select ENSP00000355316.2:n.1325-22904A>T
ENST00000361669.6:c.1325-22904A>T ENSP00000355316.2:n.1325-22904A>T
ENST00000439827.1:c.1324+28819A>T ENSP00000398767.1:n.1324+28819A>T
NM_000840.2:c.1325-22904A>T NP_000831.2:n.1325-22904A>T
XM_011516088.1:c.1324+28819A>T XP_011514390.1:n.1324+28819A>T
XM_011516090.1:c.1325-17087A>T XP_011514392.1:n.1325-17087A>T
NM_001363522.1:c.1324+28819A>T NP_001350451.1:n.1324+28819A>T
NM_000840.3:c.1325-22904A>T MANE Select NP_000831.2:n.1325-22904A>T
NM_001363522.2:c.1324+28819A>T NP_001350451.1:n.1324+28819A>T