Canonical Allele Identifier: CA3594585
Gene: GRM6 HGNC NCBI

Linked Data

ClinVar Variation Id: 733888
ClinVar RCV Id: RCV000909247 RCV003902859
dbSNP Id: rs563976478
ExAC: 5:178421769 C / T
gnomAD v2: 5-178421769-C-T
gnomAD v3: 5-178994768-C-T
gnomAD v4: 5-178994768-C-T
MyVariant Identifiers: chr5:g.178421769C>T (hg19) chr5:g.178994768C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994768C>T , CM000667.2:g.178994768C>T GRCh38
NC_000005.9:g.178421769C>T , CM000667.1:g.178421769C>T GRCh37
NC_000005.8:g.178354375C>T NCBI36
NG_008105.1:g.5356G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.177G>A MANE Select ENSP00000430767.1:p.Gln59=
ENST00000650031.1:c.177G>A ENSP00000497110.1:p.Gln59=
ENST00000231188.9:c.177G>A ENSP00000231188.5:p.Gln59=
ENST00000517717.1:c.177G>A ENSP00000430767.1:p.Gln59=
NM_000843.3:c.177G>A NP_000834.2:p.Gln59=
NM_000843.4:c.177G>A MANE Select NP_000834.2:p.Gln59=
Search 100 bp 5'
Search 100 bp 3'