Canonical Allele Identifier: CA362436705
Gene: GRM6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1195012
ClinVar RCV Id: RCV001557939
dbSNP Id: rs2113347929

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994664C>G , CM000667.2:g.178994664C>G GRCh38
NC_000005.9:g.178421665C>G , CM000667.1:g.178421665C>G GRCh37
NC_000005.8:g.178354271C>G NCBI36
NG_008105.1:g.5460G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.281G>C MANE Select ENSP00000430767.1:p.Arg94Pro
ENST00000650031.1:c.281G>C ENSP00000497110.1:p.Arg94Pro
ENST00000231188.9:c.281G>C ENSP00000231188.5:p.Arg94Pro
ENST00000517717.1:c.281G>C ENSP00000430767.1:p.Arg94Pro
NM_000843.3:c.281G>C NP_000834.2:p.Arg94Pro
NM_000843.4:c.281G>C MANE Select NP_000834.2:p.Arg94Pro