Canonical Allele Identifier: CA1723318242
Gene: GRM3 HGNC NCBI

Linked Data

dbSNP Id: rs1797999681

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815589dup , CM000669.2:g.86815589dup GRCh38
NC_000007.13:g.86444905dup , CM000669.1:g.86444905dup GRCh37
NC_000007.12:g.86282841dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-23250dup MANE Select ENSP00000355316.2:n.1325-23250dup
ENST00000361669.6:c.1325-23250dup ENSP00000355316.2:n.1325-23250dup
ENST00000439827.1:c.1324+28473dup ENSP00000398767.1:n.1324+28473dup
NM_000840.2:c.1325-23250dup NP_000831.2:n.1325-23250dup
XM_011516088.1:c.1324+28473dup XP_011514390.1:n.1324+28473dup
XM_011516090.1:c.1325-17433dup XP_011514392.1:n.1325-17433dup
NM_001363522.1:c.1324+28473dup NP_001350451.1:n.1324+28473dup
NM_000840.3:c.1325-23250dup MANE Select NP_000831.2:n.1325-23250dup
NM_001363522.2:c.1324+28473dup NP_001350451.1:n.1324+28473dup