Canonical Allele Identifier: CA162449269

Gene: GRM3

Linked Data

• dbSNP Id: rs2189812
• MyVariant Identifiers: chr7:g.86719683C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86719683C>A , CM000669.2:g.86719683C>A	GRCh38
NC_000007.13:g.86348999C>A , CM000669.1:g.86348999C>A	GRCh37
NC_000007.12:g.86186935C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.-140-45323C>A MANE Select	ENSP00000355316.2:n.-140-45323C>A
ENST00000361669.6:c.-140-45323C>A	ENSP00000355316.2:n.-140-45323C>A
ENST00000421579.1:c.-140-45323C>A	ENSP00000390037.1:n.-140-45323C>A
ENST00000439827.1:c.-140-45323C>A	ENSP00000398767.1:n.-140-45323C>A
ENST00000441140.1:c.-141+9478C>A	ENSP00000407490.1:n.-141+9478C>A
ENST00000454217.1:c.85-66578C>A	ENSP00000405427.1:n.85-66578C>A
NM_000840.2:c.-140-45323C>A	NP_000831.2:n.-140-45323C>A
XM_011516088.1:c.-140-45323C>A	XP_011514390.1:n.-140-45323C>A
XM_011516089.1:c.-140-45323C>A	XP_011514391.1:n.-140-45323C>A
XM_011516090.1:c.-140-45323C>A	XP_011514392.1:n.-140-45323C>A
NM_001363522.1:c.-140-45323C>A	NP_001350451.1:n.-140-45323C>A
XM_017012073.2:c.-140-45323C>A	XP_016867562.1:n.-140-45323C>A
NM_000840.3:c.-140-45323C>A MANE Select	NP_000831.2:n.-140-45323C>A
NM_001363522.2:c.-140-45323C>A	NP_001350451.1:n.-140-45323C>A