Canonical Allele Identifier: CA3594129
Gene: GRM6 HGNC NCBI

Linked Data

dbSNP Id: rs754777968
ExAC: 5:178415981 C / T
gnomAD v2: 5-178415981-C-T
gnomAD v3: 5-178988980-C-T
gnomAD v4: 5-178988980-C-T
COSMIC: COSM3011244
MyVariant Identifiers: chr5:g.178415981C>T (hg19) chr5:g.178988980C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178988980C>T , CM000667.2:g.178988980C>T GRCh38
NC_000005.9:g.178415981C>T , CM000667.1:g.178415981C>T GRCh37
NC_000005.8:g.178348587C>T NCBI36
NG_008105.1:g.11144G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.1309G>A MANE Select ENSP00000430767.1:p.Asp437Asn
ENST00000650031.1:c.1309G>A ENSP00000497110.1:p.Asp437Asn
ENST00000231188.9:c.1309G>A ENSP00000231188.5:p.Asp437Asn
ENST00000517717.1:c.1309G>A ENSP00000430767.1:p.Asp437Asn
NM_000843.3:c.1309G>A NP_000834.2:p.Asp437Asn
XR_941310.1:n.1470-767C>T
NM_000843.4:c.1309G>A MANE Select NP_000834.2:p.Asp437Asn
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