Canonical Allele Identifier: CA362436868
Gene: GRM6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2196529
ClinVar RCV Id: RCV002651103
dbSNP Id: rs1415659265

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994744G>T , CM000667.2:g.178994744G>T GRCh38
NC_000005.9:g.178421745G>T , CM000667.1:g.178421745G>T GRCh37
NC_000005.8:g.178354351G>T NCBI36
NG_008105.1:g.5380C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.201C>A MANE Select ENSP00000430767.1:p.His67Gln
ENST00000650031.1:c.201C>A ENSP00000497110.1:p.His67Gln
ENST00000231188.9:c.201C>A ENSP00000231188.5:p.His67Gln
ENST00000517717.1:c.201C>A ENSP00000430767.1:p.His67Gln
NM_000843.3:c.201C>A NP_000834.2:p.His67Gln
NM_000843.4:c.201C>A MANE Select NP_000834.2:p.His67Gln