Canonical Allele Identifier: CA1723318190

Gene: GRM3

Linked Data

• dbSNP Id: rs1797997086

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86815469C>T , CM000669.2:g.86815469C>T	GRCh38
NC_000007.13:g.86444785C>T , CM000669.1:g.86444785C>T	GRCh37
NC_000007.12:g.86282721C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.1325-23370C>T MANE Select	ENSP00000355316.2:n.1325-23370C>T
ENST00000361669.6:c.1325-23370C>T	ENSP00000355316.2:n.1325-23370C>T
ENST00000439827.1:c.1324+28353C>T	ENSP00000398767.1:n.1324+28353C>T
NM_000840.2:c.1325-23370C>T	NP_000831.2:n.1325-23370C>T
XM_011516088.1:c.1324+28353C>T	XP_011514390.1:n.1324+28353C>T
XM_011516089.1:c.*222C>T	XP_011514391.1:n.*222C>T
XM_011516090.1:c.1325-17553C>T	XP_011514392.1:n.1325-17553C>T
NM_001363522.1:c.1324+28353C>T	NP_001350451.1:n.1324+28353C>T
NM_000840.3:c.1325-23370C>T MANE Select	NP_000831.2:n.1325-23370C>T
NM_001363522.2:c.1324+28353C>T	NP_001350451.1:n.1324+28353C>T