Canonical Allele Identifier: CA1723306592
Gene: GRM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86804135A= , CM000669.2:g.86804135A= GRCh38
NC_000007.13:g.86433451A= , CM000669.1:g.86433451A= GRCh37
NC_000007.12:g.86271387A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_000840.3:c.1324+17019A= MANE Select NP_000831.2:n.1324+17019A=
ENST00000361669.7:c.1324+17019A= MANE Select ENSP00000355316.2:n.1324+17019A=
NM_000840.2:c.1324+17019A= NP_000831.2:n.1324+17019A=
NM_001363522.1:c.1324+17019A= NP_001350451.1:n.1324+17019A=
NM_001363522.2:c.1324+17019A= NP_001350451.1:n.1324+17019A=
ENST00000361669.6:c.1324+17019A= ENSP00000355316.2:n.1324+17019A=
ENST00000439827.1:c.1324+17019A= ENSP00000398767.1:n.1324+17019A=
XM_011516088.1:c.1324+17019A= XP_011514390.1:n.1324+17019A=
XM_011516089.1:c.1325-10952A= XP_011514391.1:n.1325-10952A=
XM_011516090.1:c.1324+17019A= XP_011514392.1:n.1324+17019A=