Canonical Allele Identifier: CA575839397

Gene: GRM3

Linked Data

• dbSNP Id: rs1221973966
• gnomAD v2: 7-86445310-T-G
• gnomAD v3: 7-86815994-T-G
• gnomAD v4: 7-86815994-T-G
• MyVariant Identifiers: chr7:g.86445310T>G (hg19) ; chr7:g.86815994T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86815994T>G , CM000669.2:g.86815994T>G	GRCh38
NC_000007.13:g.86445310T>G , CM000669.1:g.86445310T>G	GRCh37
NC_000007.12:g.86283246T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.1325-22845T>G MANE Select	ENSP00000355316.2:n.1325-22845T>G
ENST00000361669.6:c.1325-22845T>G	ENSP00000355316.2:n.1325-22845T>G
ENST00000439827.1:c.1324+28878T>G	ENSP00000398767.1:n.1324+28878T>G
NM_000840.2:c.1325-22845T>G	NP_000831.2:n.1325-22845T>G
XM_011516088.1:c.1324+28878T>G	XP_011514390.1:n.1324+28878T>G
XM_011516090.1:c.1325-17028T>G	XP_011514392.1:n.1325-17028T>G
NM_001363522.1:c.1324+28878T>G	NP_001350451.1:n.1324+28878T>G
NM_000840.3:c.1325-22845T>G MANE Select	NP_000831.2:n.1325-22845T>G
NM_001363522.2:c.1324+28878T>G	NP_001350451.1:n.1324+28878T>G