Canonical Allele Identifier: CA162034911

Gene: GRM3

Linked Data

• dbSNP Id: rs1010068021
• gnomAD v2: 7-86444991-T-C
• gnomAD v3: 7-86815675-T-C
• gnomAD v4: 7-86815675-T-C
• MyVariant Identifiers: chr7:g.86444991T>C (hg19) ; chr7:g.86815675T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.86815675T>C , CM000669.2:g.86815675T>C	GRCh38
NC_000007.13:g.86444991T>C , CM000669.1:g.86444991T>C	GRCh37
NC_000007.12:g.86282927T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361669.7:c.1325-23164T>C MANE Select	ENSP00000355316.2:n.1325-23164T>C
ENST00000361669.6:c.1325-23164T>C	ENSP00000355316.2:n.1325-23164T>C
ENST00000439827.1:c.1324+28559T>C	ENSP00000398767.1:n.1324+28559T>C
NM_000840.2:c.1325-23164T>C	NP_000831.2:n.1325-23164T>C
XM_011516088.1:c.1324+28559T>C	XP_011514390.1:n.1324+28559T>C
XM_011516090.1:c.1325-17347T>C	XP_011514392.1:n.1325-17347T>C
NM_001363522.1:c.1324+28559T>C	NP_001350451.1:n.1324+28559T>C
NM_000840.3:c.1325-23164T>C MANE Select	NP_000831.2:n.1325-23164T>C
NM_001363522.2:c.1324+28559T>C	NP_001350451.1:n.1324+28559T>C