Canonical Allele Identifier: CA2676848251
Gene: GRM6 HGNC NCBI

Linked Data

dbSNP Id: rs2113348510

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994837del , CM000667.2:g.178994837del GRCh38
NC_000005.9:g.178421838del , CM000667.1:g.178421838del GRCh37
NC_000005.8:g.178354444del NCBI36
NG_008105.1:g.5289del

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.110del MANE Select ENSP00000430767.1:p.Gly37AlafsTer3
ENST00000650031.1:c.110del ENSP00000497110.1:p.Gly37AlafsTer3
ENST00000231188.9:c.110del ENSP00000231188.5:p.Gly37AlafsTer3
ENST00000517717.1:c.110del ENSP00000430767.1:p.Gly37AlafsTer3
NM_000843.3:c.110del NP_000834.2:p.Gly37AlafsTer3
NM_000843.4:c.110del MANE Select NP_000834.2:p.Gly37AlafsTer3