Canonical Allele Identifier: CA162034930

Gene: GRM3

Linked Data

• dbSNP Id: rs753579144
• gnomAD v2: 7-86445031-A-G
• gnomAD v3: 7-86815715-A-G
• gnomAD v4: 7-86815715-A-G
• MyVariant Identifiers: chr7:g.86445031A>G (hg19) ; chr7:g.86815715A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86815715A>G , CM000669.2:g.86815715A>G	GRCh38
NC_000007.13:g.86445031A>G , CM000669.1:g.86445031A>G	GRCh37
NC_000007.12:g.86282967A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.1325-23124A>G MANE Select	ENSP00000355316.2:n.1325-23124A>G
ENST00000361669.6:c.1325-23124A>G	ENSP00000355316.2:n.1325-23124A>G
ENST00000439827.1:c.1324+28599A>G	ENSP00000398767.1:n.1324+28599A>G
NM_000840.2:c.1325-23124A>G	NP_000831.2:n.1325-23124A>G
XM_011516088.1:c.1324+28599A>G	XP_011514390.1:n.1324+28599A>G
XM_011516090.1:c.1325-17307A>G	XP_011514392.1:n.1325-17307A>G
NM_001363522.1:c.1324+28599A>G	NP_001350451.1:n.1324+28599A>G
NM_000840.3:c.1325-23124A>G MANE Select	NP_000831.2:n.1325-23124A>G
NM_001363522.2:c.1324+28599A>G	NP_001350451.1:n.1324+28599A>G