Canonical Allele Identifier: CA362436739

Gene: GRM6

Linked Data

• gnomAD v4: 5-178994682-C-A
• MyVariant Identifiers: chr5:g.178421683C>A (hg19) ; chr5:g.178994682C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.178994682C>A , CM000667.2:g.178994682C>A	GRCh38
NC_000005.9:g.178421683C>A , CM000667.1:g.178421683C>A	GRCh37
NC_000005.8:g.178354289C>A	NCBI36
NG_008105.1:g.5442G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517717.3:c.263G>T MANE Select	ENSP00000430767.1:p.Gly88Val
ENST00000650031.1:c.263G>T	ENSP00000497110.1:p.Gly88Val
ENST00000231188.9:c.263G>T	ENSP00000231188.5:p.Gly88Val
ENST00000517717.1:c.263G>T	ENSP00000430767.1:p.Gly88Val
NM_000843.3:c.263G>T	NP_000834.2:p.Gly88Val
NM_000843.4:c.263G>T MANE Select	NP_000834.2:p.Gly88Val