Canonical Allele Identifier: CA843303922

Gene: GRM3

Linked Data

• dbSNP Id: rs724226
• MyVariant Identifiers: chr7:g.86325374A>T (hg19) ; chr7:g.86696058A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86696058A>T , CM000669.2:g.86696058A>T	GRCh38
NC_000007.13:g.86325374A>T , CM000669.1:g.86325374A>T	GRCh37
NC_000007.12:g.86163310A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361669.7:c.-141+51186A>T MANE Select	ENSP00000355316.2:n.-141+51186A>T
ENST00000361669.6:c.-141+51186A>T	ENSP00000355316.2:n.-141+51186A>T
ENST00000421579.1:c.-141+51087A>T	ENSP00000390037.1:n.-141+51087A>T
ENST00000439827.1:c.-141+51186A>T	ENSP00000398767.1:n.-141+51186A>T
ENST00000454217.1:c.84+51186A>T	ENSP00000405427.1:n.84+51186A>T
NM_000840.2:c.-141+51186A>T	NP_000831.2:n.-141+51186A>T
XM_011516088.1:c.-141+51186A>T	XP_011514390.1:n.-141+51186A>T
XM_011516089.1:c.-141+51186A>T	XP_011514391.1:n.-141+51186A>T
XM_011516090.1:c.-141+51186A>T	XP_011514392.1:n.-141+51186A>T
NM_001363522.1:c.-141+51186A>T	NP_001350451.1:n.-141+51186A>T
XM_017012073.2:c.-141+51186A>T	XP_016867562.1:n.-141+51186A>T
NM_000840.3:c.-141+51186A>T MANE Select	NP_000831.2:n.-141+51186A>T
NM_001363522.2:c.-141+51186A>T	NP_001350451.1:n.-141+51186A>T