Canonical Allele Identifier: CA1723318256
Gene: GRM3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815639A= , CM000669.2:g.86815639A= GRCh38
NC_000007.13:g.86444955A= , CM000669.1:g.86444955A= GRCh37
NC_000007.12:g.86282891A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-23200A= MANE Select ENSP00000355316.2:n.1325-23200A=
ENST00000361669.6:c.1325-23200A= ENSP00000355316.2:n.1325-23200A=
ENST00000439827.1:c.1324+28523A= ENSP00000398767.1:n.1324+28523A=
NM_000840.2:c.1325-23200A= NP_000831.2:n.1325-23200A=
XM_011516088.1:c.1324+28523A= XP_011514390.1:n.1324+28523A=
XM_011516090.1:c.1325-17383A= XP_011514392.1:n.1325-17383A=
NM_001363522.1:c.1324+28523A= NP_001350451.1:n.1324+28523A=
NM_000840.3:c.1325-23200A= MANE Select NP_000831.2:n.1325-23200A=
NM_001363522.2:c.1324+28523A= NP_001350451.1:n.1324+28523A=
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