Canonical Allele Identifier: CA162034849

Gene: GRM3

Linked Data

• dbSNP Id: rs1035435568
• gnomAD v3: 7-86815463-T-A
• gnomAD v4: 7-86815463-T-A
• MyVariant Identifiers: chr7:g.86444779T>A (hg19) ; chr7:g.86815463T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86815463T>A , CM000669.2:g.86815463T>A	GRCh38
NC_000007.13:g.86444779T>A , CM000669.1:g.86444779T>A	GRCh37
NC_000007.12:g.86282715T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.1325-23376T>A MANE Select	ENSP00000355316.2:n.1325-23376T>A
ENST00000361669.6:c.1325-23376T>A	ENSP00000355316.2:n.1325-23376T>A
ENST00000439827.1:c.1324+28347T>A	ENSP00000398767.1:n.1324+28347T>A
NM_000840.2:c.1325-23376T>A	NP_000831.2:n.1325-23376T>A
XM_011516088.1:c.1324+28347T>A	XP_011514390.1:n.1324+28347T>A
XM_011516089.1:c.*216T>A	XP_011514391.1:n.*216T>A
XM_011516090.1:c.1325-17559T>A	XP_011514392.1:n.1325-17559T>A
NM_001363522.1:c.1324+28347T>A	NP_001350451.1:n.1324+28347T>A
NM_000840.3:c.1325-23376T>A MANE Select	NP_000831.2:n.1325-23376T>A
NM_001363522.2:c.1324+28347T>A	NP_001350451.1:n.1324+28347T>A