Canonical Allele Identifier: CA362437031
Gene: GRM6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1399164
ClinVar RCV Id: RCV001915417
dbSNP Id: rs2113348491

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994826G>A , CM000667.2:g.178994826G>A GRCh38
NC_000005.9:g.178421827G>A , CM000667.1:g.178421827G>A GRCh37
NC_000005.8:g.178354433G>A NCBI36
NG_008105.1:g.5298C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.119C>T MANE Select ENSP00000430767.1:p.Thr40Met
ENST00000650031.1:c.119C>T ENSP00000497110.1:p.Thr40Met
ENST00000231188.9:c.119C>T ENSP00000231188.5:p.Thr40Met
ENST00000517717.1:c.119C>T ENSP00000430767.1:p.Thr40Met
NM_000843.3:c.119C>T NP_000834.2:p.Thr40Met
NM_000843.4:c.119C>T MANE Select NP_000834.2:p.Thr40Met