Canonical Allele Identifier: CA1723318262
Gene: GRM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815649T= , CM000669.2:g.86815649T= GRCh38
NC_000007.13:g.86444965T= , CM000669.1:g.86444965T= GRCh37
NC_000007.12:g.86282901T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-23190T= MANE Select ENSP00000355316.2:n.1325-23190T=
ENST00000361669.6:c.1325-23190T= ENSP00000355316.2:n.1325-23190T=
ENST00000439827.1:c.1324+28533T= ENSP00000398767.1:n.1324+28533T=
NM_000840.2:c.1325-23190T= NP_000831.2:n.1325-23190T=
XM_011516088.1:c.1324+28533T= XP_011514390.1:n.1324+28533T=
XM_011516090.1:c.1325-17373T= XP_011514392.1:n.1325-17373T=
NM_001363522.1:c.1324+28533T= NP_001350451.1:n.1324+28533T=
NM_000840.3:c.1325-23190T= MANE Select NP_000831.2:n.1325-23190T=
NM_001363522.2:c.1324+28533T= NP_001350451.1:n.1324+28533T=