Canonical Allele Identifier: CA1723318282
Gene: GRM3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815688C= , CM000669.2:g.86815688C= GRCh38
NC_000007.13:g.86445004C= , CM000669.1:g.86445004C= GRCh37
NC_000007.12:g.86282940C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-23151C= MANE Select ENSP00000355316.2:n.1325-23151C=
ENST00000361669.6:c.1325-23151C= ENSP00000355316.2:n.1325-23151C=
ENST00000439827.1:c.1324+28572C= ENSP00000398767.1:n.1324+28572C=
NM_000840.2:c.1325-23151C= NP_000831.2:n.1325-23151C=
XM_011516088.1:c.1324+28572C= XP_011514390.1:n.1324+28572C=
XM_011516090.1:c.1325-17334C= XP_011514392.1:n.1325-17334C=
NM_001363522.1:c.1324+28572C= NP_001350451.1:n.1324+28572C=
NM_000840.3:c.1325-23151C= MANE Select NP_000831.2:n.1325-23151C=
NM_001363522.2:c.1324+28572C= NP_001350451.1:n.1324+28572C=
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