Canonical Allele Identifier: CA1723318365
Gene: GRM3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815881C= , CM000669.2:g.86815881C= GRCh38
NC_000007.13:g.86445197C= , CM000669.1:g.86445197C= GRCh37
NC_000007.12:g.86283133C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-22958C= MANE Select ENSP00000355316.2:n.1325-22958C=
ENST00000361669.6:c.1325-22958C= ENSP00000355316.2:n.1325-22958C=
ENST00000439827.1:c.1324+28765C= ENSP00000398767.1:n.1324+28765C=
NM_000840.2:c.1325-22958C= NP_000831.2:n.1325-22958C=
XM_011516088.1:c.1324+28765C= XP_011514390.1:n.1324+28765C=
XM_011516090.1:c.1325-17141C= XP_011514392.1:n.1325-17141C=
NM_001363522.1:c.1324+28765C= NP_001350451.1:n.1324+28765C=
NM_000840.3:c.1325-22958C= MANE Select NP_000831.2:n.1325-22958C=
NM_001363522.2:c.1324+28765C= NP_001350451.1:n.1324+28765C=
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