Canonical Allele Identifier: CA1723318184
Gene: GRM3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815453G= , CM000669.2:g.86815453G= GRCh38
NC_000007.13:g.86444769G= , CM000669.1:g.86444769G= GRCh37
NC_000007.12:g.86282705G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-23386G= MANE Select ENSP00000355316.2:n.1325-23386G=
ENST00000361669.6:c.1325-23386G= ENSP00000355316.2:n.1325-23386G=
ENST00000439827.1:c.1324+28337G= ENSP00000398767.1:n.1324+28337G=
NM_000840.2:c.1325-23386G= NP_000831.2:n.1325-23386G=
XM_011516088.1:c.1324+28337G= XP_011514390.1:n.1324+28337G=
XM_011516089.1:c.*206G= XP_011514391.1:n.*206G=
XM_011516090.1:c.1325-17569G= XP_011514392.1:n.1325-17569G=
NM_001363522.1:c.1324+28337G= NP_001350451.1:n.1324+28337G=
NM_000840.3:c.1325-23386G= MANE Select NP_000831.2:n.1325-23386G=
NM_001363522.2:c.1324+28337G= NP_001350451.1:n.1324+28337G=
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