Canonical Allele Identifier: CA362436787
Gene: GRM6 HGNC NCBI

Linked Data

dbSNP Id: rs1472481615

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994706T>C , CM000667.2:g.178994706T>C GRCh38
NC_000005.9:g.178421707T>C , CM000667.1:g.178421707T>C GRCh37
NC_000005.8:g.178354313T>C NCBI36
NG_008105.1:g.5418A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.239A>G MANE Select ENSP00000430767.1:p.Asn80Ser
ENST00000650031.1:c.239A>G ENSP00000497110.1:p.Asn80Ser
ENST00000231188.9:c.239A>G ENSP00000231188.5:p.Asn80Ser
ENST00000517717.1:c.239A>G ENSP00000430767.1:p.Asn80Ser
NM_000843.3:c.239A>G NP_000834.2:p.Asn80Ser
NM_000843.4:c.239A>G MANE Select NP_000834.2:p.Asn80Ser