Canonical Allele Identifier: CA1723318220
Gene: GRM3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815540T= , CM000669.2:g.86815540T= GRCh38
NC_000007.13:g.86444856T= , CM000669.1:g.86444856T= GRCh37
NC_000007.12:g.86282792T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-23299T= MANE Select ENSP00000355316.2:n.1325-23299T=
ENST00000361669.6:c.1325-23299T= ENSP00000355316.2:n.1325-23299T=
ENST00000439827.1:c.1324+28424T= ENSP00000398767.1:n.1324+28424T=
NM_000840.2:c.1325-23299T= NP_000831.2:n.1325-23299T=
XM_011516088.1:c.1324+28424T= XP_011514390.1:n.1324+28424T=
XM_011516090.1:c.1325-17482T= XP_011514392.1:n.1325-17482T=
NM_001363522.1:c.1324+28424T= NP_001350451.1:n.1324+28424T=
NM_000840.3:c.1325-23299T= MANE Select NP_000831.2:n.1325-23299T=
NM_001363522.2:c.1324+28424T= NP_001350451.1:n.1324+28424T=
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