Canonical Allele Identifier: CA12293678
Gene: GRM4 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.34022670T>C
GRCh37 chr6:g.33990447T>C
gnomAD v2:
6:33990447 T / C
gnomAD v3:
6:34022670 T / C
gnomAD v4:
chr6-34022670-T-C
Joint Max Group AF 0.63465748 (AFR)
Genomes Max Group AF 0.6320308 (AFR)
Exomes Max Group AF 0.63420692 (AFR)
dbSNP:
2229901
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.34022670T>C , CM000668.2:g.34022670T>C GRCh38
NC_000006.11:g.33990447T>C , CM000668.1:g.33990447T>C GRCh37
NC_000006.10:g.34098425T>C NCBI36
NG_029677.3:g.137953A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000538487.7:c.*151A>G MANE Select ENSP00000440556.1:n.*151A>G
ENST00000374177.7:c.*151A>G ENSP00000363292.3:n.*151A>G
ENST00000374181.8:c.*151A>G ENSP00000363296.4:n.*151A>G
ENST00000455714.6:c.*151A>G ENSP00000398456.2:n.*151A>G
ENST00000535756.5:c.*151A>G ENSP00000437925.1:n.*151A>G
ENST00000538487.6:c.*151A>G ENSP00000440556.1:n.*151A>G
ENST00000544773.6:c.*151A>G ENSP00000437730.1:n.*151A>G
ENST00000545715.5:n.2939A>G
ENST00000609222.5:c.*151A>G ENSP00000477466.1:n.*151A>G
ENST00000609860.5:n.3365A>G
NM_000841.3:c.*151A>G NP_000832.1:n.*151A>G
NM_001256809.2:c.*151A>G NP_001243738.1:n.*151A>G
NM_001256811.2:c.*151A>G NP_001243740.1:n.*151A>G
NM_001256812.2:c.*151A>G NP_001243741.1:n.*151A>G
NM_001256813.2:c.*151A>G NP_001243742.1:n.*151A>G
NM_001282847.1:c.*151A>G NP_001269776.1:n.*151A>G
XM_011514531.1:c.*151A>G XP_011512833.1:n.*151A>G
XM_017010790.2:c.*151A>G XP_016866279.1:n.*151A>G
XM_017010791.2:c.*151A>G XP_016866280.1:n.*151A>G
XM_017010792.1:c.*151A>G XP_016866281.1:n.*151A>G
XM_017010793.2:c.*151A>G XP_016866282.1:n.*151A>G
XR_001743363.1:n.3879A>G
XR_001743364.2:n.3495A>G
NM_000841.4:c.*151A>G MANE Select NP_000832.1:n.*151A>G
NM_001256813.3:c.*151A>G NP_001243742.1:n.*151A>G
NM_001282847.2:c.*151A>G NP_001269776.1:n.*151A>G
NM_001256809.3:c.*151A>G NP_001243738.1:n.*151A>G
NM_001256811.3:c.*151A>G NP_001243740.1:n.*151A>G
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