Canonical Allele Identifier: CA843335603

Gene: GRM3

Linked Data

• dbSNP Id: rs1270501641
• gnomAD v3: 7-86815465-A-G
• gnomAD v4: 7-86815465-A-G
• MyVariant Identifiers: chr7:g.86444781A>G (hg19) ; chr7:g.86815465A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86815465A>G , CM000669.2:g.86815465A>G	GRCh38
NC_000007.13:g.86444781A>G , CM000669.1:g.86444781A>G	GRCh37
NC_000007.12:g.86282717A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.1325-23374A>G MANE Select	ENSP00000355316.2:n.1325-23374A>G
ENST00000361669.6:c.1325-23374A>G	ENSP00000355316.2:n.1325-23374A>G
ENST00000439827.1:c.1324+28349A>G	ENSP00000398767.1:n.1324+28349A>G
NM_000840.2:c.1325-23374A>G	NP_000831.2:n.1325-23374A>G
XM_011516088.1:c.1324+28349A>G	XP_011514390.1:n.1324+28349A>G
XM_011516089.1:c.*218A>G	XP_011514391.1:n.*218A>G
XM_011516090.1:c.1325-17557A>G	XP_011514392.1:n.1325-17557A>G
NM_001363522.1:c.1324+28349A>G	NP_001350451.1:n.1324+28349A>G
NM_000840.3:c.1325-23374A>G MANE Select	NP_000831.2:n.1325-23374A>G
NM_001363522.2:c.1324+28349A>G	NP_001350451.1:n.1324+28349A>G