Canonical Allele Identifier: CA162034870

Gene: GRM3

Linked Data

• dbSNP Id: rs930795122
• gnomAD v3: 7-86815517-C-T
• gnomAD v4: 7-86815517-C-T
• MyVariant Identifiers: chr7:g.86444833C>T (hg19) ; chr7:g.86815517C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86815517C>T , CM000669.2:g.86815517C>T	GRCh38
NC_000007.13:g.86444833C>T , CM000669.1:g.86444833C>T	GRCh37
NC_000007.12:g.86282769C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.1325-23322C>T MANE Select	ENSP00000355316.2:n.1325-23322C>T
ENST00000361669.6:c.1325-23322C>T	ENSP00000355316.2:n.1325-23322C>T
ENST00000439827.1:c.1324+28401C>T	ENSP00000398767.1:n.1324+28401C>T
NM_000840.2:c.1325-23322C>T	NP_000831.2:n.1325-23322C>T
XM_011516088.1:c.1324+28401C>T	XP_011514390.1:n.1324+28401C>T
XM_011516090.1:c.1325-17505C>T	XP_011514392.1:n.1325-17505C>T
NM_001363522.1:c.1324+28401C>T	NP_001350451.1:n.1324+28401C>T
NM_000840.3:c.1325-23322C>T MANE Select	NP_000831.2:n.1325-23322C>T
NM_001363522.2:c.1324+28401C>T	NP_001350451.1:n.1324+28401C>T