Canonical Allele Identifier: CA843326398

Gene: GRM3

Linked Data

• dbSNP Id: rs10234440
• gnomAD v3: 7-86791061-T-G
• gnomAD v4: 7-86791061-T-G
• MyVariant Identifiers: chr7:g.86420377T>G (hg19) ; chr7:g.86791061T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86791061T>G , CM000669.2:g.86791061T>G	GRCh38
NC_000007.13:g.86420377T>G , CM000669.1:g.86420377T>G	GRCh37
NC_000007.12:g.86258313T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361669.7:c.1324+3945T>G MANE Select	ENSP00000355316.2:n.1324+3945T>G
ENST00000361669.6:c.1324+3945T>G	ENSP00000355316.2:n.1324+3945T>G
ENST00000439827.1:c.1324+3945T>G	ENSP00000398767.1:n.1324+3945T>G
NM_000840.2:c.1324+3945T>G	NP_000831.2:n.1324+3945T>G
XM_011516088.1:c.1324+3945T>G	XP_011514390.1:n.1324+3945T>G
XM_011516089.1:c.1324+3945T>G	XP_011514391.1:n.1324+3945T>G
XM_011516090.1:c.1324+3945T>G	XP_011514392.1:n.1324+3945T>G
XR_927721.1:n.1425+2126A>C
NM_001363522.1:c.1324+3945T>G	NP_001350451.1:n.1324+3945T>G
XM_017012073.2:c.1325-1987T>G	XP_016867562.1:n.1325-1987T>G
XR_002956570.1:n.90+2126A>C
XR_002956571.1:n.88+3559A>C
NM_000840.3:c.1324+3945T>G MANE Select	NP_000831.2:n.1324+3945T>G
NM_001363522.2:c.1324+3945T>G	NP_001350451.1:n.1324+3945T>G