Canonical Allele Identifier: CA575839359

Gene: GRM3

Linked Data

• dbSNP Id: rs1227786234
• gnomAD v2: 7-86444770-T-C
• gnomAD v3: 7-86815454-T-C
• gnomAD v4: 7-86815454-T-C
• MyVariant Identifiers: chr7:g.86444770T>C (hg19) ; chr7:g.86815454T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86815454T>C , CM000669.2:g.86815454T>C	GRCh38
NC_000007.13:g.86444770T>C , CM000669.1:g.86444770T>C	GRCh37
NC_000007.12:g.86282706T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.1325-23385T>C MANE Select	ENSP00000355316.2:n.1325-23385T>C
ENST00000361669.6:c.1325-23385T>C	ENSP00000355316.2:n.1325-23385T>C
ENST00000439827.1:c.1324+28338T>C	ENSP00000398767.1:n.1324+28338T>C
NM_000840.2:c.1325-23385T>C	NP_000831.2:n.1325-23385T>C
XM_011516088.1:c.1324+28338T>C	XP_011514390.1:n.1324+28338T>C
XM_011516089.1:c.*207T>C	XP_011514391.1:n.*207T>C
XM_011516090.1:c.1325-17568T>C	XP_011514392.1:n.1325-17568T>C
NM_001363522.1:c.1324+28338T>C	NP_001350451.1:n.1324+28338T>C
NM_000840.3:c.1325-23385T>C MANE Select	NP_000831.2:n.1325-23385T>C
NM_001363522.2:c.1324+28338T>C	NP_001350451.1:n.1324+28338T>C