Canonical Allele Identifier: CA15503050
Gene: GRM3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17161018

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815615G>A , CM000669.2:g.86815615G>A GRCh38
NC_000007.13:g.86444931G>A , CM000669.1:g.86444931G>A GRCh37
NC_000007.12:g.86282867G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_000840.2:c.1325-23224G>A VV NP_000831.2:p.=
XM_011516088.1:c.1324+28499G>A XP_011514390.1:p.=
XM_011516090.1:c.1325-17407G>A XP_011514392.1:p.=
NM_001363522.1:c.1324+28499G>A VV NP_001350451.1:p.=
ENST00000361669.6:c.1325-23224G>A ENSP00000355316.2:p.=
ENST00000439827.1:c.1324+28499G>A ENSP00000398767.1:p.=