Canonical Allele Identifier: CA564902054
Gene: GRM6 HGNC NCBI

Linked Data

dbSNP Id: rs1291641161
gnomAD v2: 5-178421696-CG-C
gnomAD v4: 5-178994695-CG-C
MyVariant Identifiers: chr5:g.178421697del (hg19) chr5:g.178994696del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994699del , CM000667.2:g.178994699del GRCh38
NC_000005.9:g.178421700del , CM000667.1:g.178421700del GRCh37
NC_000005.8:g.178354306del NCBI36
NG_008105.1:g.5428del

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.249del MANE Select ENSP00000430767.1:p.Glu84SerfsTer27
ENST00000650031.1:c.249del ENSP00000497110.1:p.Glu84SerfsTer27
ENST00000231188.9:c.249del ENSP00000231188.5:p.Glu84SerfsTer27
ENST00000517717.1:c.249del ENSP00000430767.1:p.Glu84SerfsTer27
NM_000843.3:c.249del NP_000834.2:p.Glu84SerfsTer27
NM_000843.4:c.249del MANE Select NP_000834.2:p.Glu84SerfsTer27
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