Canonical Allele Identifier: CA4323922
Gene: GRM3 HGNC NCBI
MyVariant.info:
GRCh38 chr7:g.86644771G>A
GRCh37 chr7:g.86274087G>A
gnomAD v2:
7:86274087 G / A
gnomAD v3:
7:86644771 G / A
gnomAD v4:
chr7-86644771-G-A
Joint Max Group AF 0.01387927 (SAS)
Genomes Max Group AF 0.01308039 (SAS)
Exomes Max Group AF 0.01377294 (SAS)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86644771G>A , CM000669.2:g.86644771G>A GRCh38
NC_000007.13:g.86274087G>A , CM000669.1:g.86274087G>A GRCh37
NC_000007.12:g.86112023G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.-242G>A MANE Select ENSP00000355316.2:n.-242G>A
ENST00000361669.6:c.-242G>A ENSP00000355316.2:n.-242G>A
ENST00000454217.1:c.-18G>A ENSP00000405427.1:n.-18G>A
NM_000840.2:c.-242G>A NP_000831.2:n.-242G>A
XM_011516088.1:c.-242G>A XP_011514390.1:n.-242G>A
XM_011516089.1:c.-242G>A XP_011514391.1:n.-242G>A
XM_011516090.1:c.-242G>A XP_011514392.1:n.-242G>A
NM_001363522.1:c.-242G>A NP_001350451.1:n.-242G>A
XM_017012073.2:c.-242G>A XP_016867562.1:n.-242G>A
NM_000840.3:c.-242G>A MANE Select NP_000831.2:n.-242G>A
NM_001363522.2:c.-242G>A NP_001350451.1:n.-242G>A
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