Canonical Allele Identifier: CA162034929

Gene: GRM3

Linked Data

• dbSNP Id: rs919419652
• gnomAD v2: 7-86445027-C-T
• gnomAD v3: 7-86815711-C-T
• gnomAD v4: 7-86815711-C-T
• MyVariant Identifiers: chr7:g.86445027C>T (hg19) ; chr7:g.86815711C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86815711C>T , CM000669.2:g.86815711C>T	GRCh38
NC_000007.13:g.86445027C>T , CM000669.1:g.86445027C>T	GRCh37
NC_000007.12:g.86282963C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.1325-23128C>T MANE Select	ENSP00000355316.2:n.1325-23128C>T
ENST00000361669.6:c.1325-23128C>T	ENSP00000355316.2:n.1325-23128C>T
ENST00000439827.1:c.1324+28595C>T	ENSP00000398767.1:n.1324+28595C>T
NM_000840.2:c.1325-23128C>T	NP_000831.2:n.1325-23128C>T
XM_011516088.1:c.1324+28595C>T	XP_011514390.1:n.1324+28595C>T
XM_011516090.1:c.1325-17311C>T	XP_011514392.1:n.1325-17311C>T
NM_001363522.1:c.1324+28595C>T	NP_001350451.1:n.1324+28595C>T
NM_000840.3:c.1325-23128C>T MANE Select	NP_000831.2:n.1325-23128C>T
NM_001363522.2:c.1324+28595C>T	NP_001350451.1:n.1324+28595C>T