Canonical Allele Identifier: CA12293678
Gene: GRM4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2229901

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