Canonical Allele Identifier: CA576123062

Gene: GRM3

Linked Data

• dbSNP Id: rs1391529285
• gnomAD v2: 7-86325302-G-A
• gnomAD v3: 7-86695986-G-A
• gnomAD v4: 7-86695986-G-A
• MyVariant Identifiers: chr7:g.86325302G>A (hg19) ; chr7:g.86695986G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86695986G>A , CM000669.2:g.86695986G>A	GRCh38
NC_000007.13:g.86325302G>A , CM000669.1:g.86325302G>A	GRCh37
NC_000007.12:g.86163238G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361669.7:c.-141+51114G>A MANE Select	ENSP00000355316.2:n.-141+51114G>A
ENST00000361669.6:c.-141+51114G>A	ENSP00000355316.2:n.-141+51114G>A
ENST00000421579.1:c.-141+51015G>A	ENSP00000390037.1:n.-141+51015G>A
ENST00000439827.1:c.-141+51114G>A	ENSP00000398767.1:n.-141+51114G>A
ENST00000454217.1:c.84+51114G>A	ENSP00000405427.1:n.84+51114G>A
NM_000840.2:c.-141+51114G>A	NP_000831.2:n.-141+51114G>A
XM_011516088.1:c.-141+51114G>A	XP_011514390.1:n.-141+51114G>A
XM_011516089.1:c.-141+51114G>A	XP_011514391.1:n.-141+51114G>A
XM_011516090.1:c.-141+51114G>A	XP_011514392.1:n.-141+51114G>A
NM_001363522.1:c.-141+51114G>A	NP_001350451.1:n.-141+51114G>A
XM_017012073.2:c.-141+51114G>A	XP_016867562.1:n.-141+51114G>A
NM_000840.3:c.-141+51114G>A MANE Select	NP_000831.2:n.-141+51114G>A
NM_001363522.2:c.-141+51114G>A	NP_001350451.1:n.-141+51114G>A