Canonical Allele Identifier: CA11547527
Gene: GRM7 HGNC NCBI

Linked Data

dbSNP Id: rs480409
gnomAD v2: 3-7010081-C-T
gnomAD v3: 3-6968394-C-T
gnomAD v4: 3-6968394-C-T
MyVariant Identifiers: chr3:g.7010081C>T (hg19) chr3:g.6968394C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.6968394C>T , CM000665.2:g.6968394C>T GRCh38
NC_000003.11:g.7010081C>T , CM000665.1:g.7010081C>T GRCh37
NC_000003.10:g.6985081C>T NCBI36
NG_029781.1:g.112280C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000357716.9:c.519+106487C>T MANE Select ENSP00000350348.4:n.519+106487C>T
ENST00000357716.8:c.519+106487C>T ENSP00000350348.4:n.519+106487C>T
ENST00000389335.7:c.519+106487C>T ENSP00000373986.3:n.519+106487C>T
ENST00000389336.8:c.519+106487C>T ENSP00000373987.4:n.519+106487C>T
ENST00000435689.5:c.74+11775C>T ENSP00000405194.1:n.74+11775C>T
ENST00000440923.7:c.519+106487C>T ENSP00000412329.3:n.519+106487C>T
ENST00000443259.1:c.*115+84088C>T ENSP00000404161.1:n.*115+84088C>T
ENST00000448328.6:c.-106+139690C>T ENSP00000393799.2:n.-106+139690C>T
ENST00000467425.5:c.519+106487C>T ENSP00000419835.1:n.519+106487C>T
ENST00000486284.5:c.519+106487C>T ENSP00000417536.1:n.519+106487C>T
NM_000844.3:c.519+106487C>T NP_000835.1:n.519+106487C>T
NM_181874.2:c.519+106487C>T NP_870989.1:n.519+106487C>T
XR_940422.1:n.811+106487C>T
XM_017006272.1:c.21+105393C>T XP_016861761.1:n.21+105393C>T
XM_017006273.1:c.21+105393C>T XP_016861762.1:n.21+105393C>T
XR_001740134.2:n.793+106487C>T
XR_001740135.2:n.793+106487C>T
XR_001740136.2:n.793+106487C>T
XR_001740137.2:n.793+106487C>T
NM_000844.4:c.519+106487C>T MANE Select NP_000835.1:n.519+106487C>T
NM_181874.3:c.519+106487C>T NP_870989.1:n.519+106487C>T
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