Canonical Allele Identifier: CA1723318397
Gene: GRM3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815976G= , CM000669.2:g.86815976G= GRCh38
NC_000007.13:g.86445292G= , CM000669.1:g.86445292G= GRCh37
NC_000007.12:g.86283228G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-22863G= MANE Select ENSP00000355316.2:n.1325-22863G=
ENST00000361669.6:c.1325-22863G= ENSP00000355316.2:n.1325-22863G=
ENST00000439827.1:c.1324+28860G= ENSP00000398767.1:n.1324+28860G=
NM_000840.2:c.1325-22863G= NP_000831.2:n.1325-22863G=
XM_011516088.1:c.1324+28860G= XP_011514390.1:n.1324+28860G=
XM_011516090.1:c.1325-17046G= XP_011514392.1:n.1325-17046G=
NM_001363522.1:c.1324+28860G= NP_001350451.1:n.1324+28860G=
NM_000840.3:c.1325-22863G= MANE Select NP_000831.2:n.1325-22863G=
NM_001363522.2:c.1324+28860G= NP_001350451.1:n.1324+28860G=
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