Canonical Allele Identifier: CA1723318182

Gene: GRM3

Linked Data

• dbSNP Id: rs1797996686

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86815449G>C , CM000669.2:g.86815449G>C	GRCh38
NC_000007.13:g.86444765G>C , CM000669.1:g.86444765G>C	GRCh37
NC_000007.12:g.86282701G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.1325-23390G>C MANE Select	ENSP00000355316.2:n.1325-23390G>C
ENST00000361669.6:c.1325-23390G>C	ENSP00000355316.2:n.1325-23390G>C
ENST00000439827.1:c.1324+28333G>C	ENSP00000398767.1:n.1324+28333G>C
NM_000840.2:c.1325-23390G>C	NP_000831.2:n.1325-23390G>C
XM_011516088.1:c.1324+28333G>C	XP_011514390.1:n.1324+28333G>C
XM_011516089.1:c.*202G>C	XP_011514391.1:n.*202G>C
XM_011516090.1:c.1325-17573G>C	XP_011514392.1:n.1325-17573G>C
NM_001363522.1:c.1324+28333G>C	NP_001350451.1:n.1324+28333G>C
NM_000840.3:c.1325-23390G>C MANE Select	NP_000831.2:n.1325-23390G>C
NM_001363522.2:c.1324+28333G>C	NP_001350451.1:n.1324+28333G>C