Canonical Allele Identifier: CA448376316

Gene: GRM6

Linked Data

• gnomAD v4: 5-178994825-C-T
• MyVariant Identifiers: chr5:g.178421826C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.178994825C>T , CM000667.2:g.178994825C>T	GRCh38
NC_000005.9:g.178421826C>T , CM000667.1:g.178421826C>T	GRCh37
NC_000005.8:g.178354432C>T	NCBI36
NG_008105.1:g.5299G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517717.3:c.120G>A MANE Select	ENSP00000430767.1:p.Thr40=
ENST00000650031.1:c.120G>A	ENSP00000497110.1:p.Thr40=
ENST00000231188.9:c.120G>A	ENSP00000231188.5:p.Thr40=
ENST00000517717.1:c.120G>A	ENSP00000430767.1:p.Thr40=
NM_000843.3:c.120G>A	NP_000834.2:p.Thr40=
NM_000843.4:c.120G>A MANE Select	NP_000834.2:p.Thr40=