Canonical Allele Identifier: CA448027915

Gene: GRM6

Linked Data

• gnomAD v4: 5-178994558-G-T
• MyVariant Identifiers: chr5:g.178421559G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.178994558G>T , CM000667.2:g.178994558G>T	GRCh38
NC_000005.9:g.178421559G>T , CM000667.1:g.178421559G>T	GRCh37
NC_000005.8:g.178354165G>T	NCBI36
NG_008105.1:g.5566C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517717.3:c.387C>A MANE Select	ENSP00000430767.1:p.Arg129=
ENST00000650031.1:c.387C>A	ENSP00000497110.1:p.Arg129=
ENST00000231188.9:c.387C>A	ENSP00000231188.5:p.Arg129=
ENST00000517717.1:c.387C>A	ENSP00000430767.1:p.Arg129=
NM_000843.3:c.387C>A	NP_000834.2:p.Arg129=
NM_000843.4:c.387C>A MANE Select	NP_000834.2:p.Arg129=