Canonical Allele Identifier: CA362430169

Gene: GRM6

Linked Data

• dbSNP Id: rs1314147656
• gnomAD v2: 5-178416086-G-T
• MyVariant Identifiers: chr5:g.178416086G>T (hg19) ; chr5:g.178989085G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.178989085G>T , CM000667.2:g.178989085G>T	GRCh38
NC_000005.9:g.178416086G>T , CM000667.1:g.178416086G>T	GRCh37
NC_000005.8:g.178348692G>T	NCBI36
NG_008105.1:g.11039C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517717.3:c.1204C>A MANE Select	ENSP00000430767.1:p.Gln402Lys
ENST00000650031.1:c.1204C>A	ENSP00000497110.1:p.Gln402Lys
ENST00000231188.9:c.1204C>A	ENSP00000231188.5:p.Gln402Lys
ENST00000517717.1:c.1204C>A	ENSP00000430767.1:p.Gln402Lys
NM_000843.3:c.1204C>A	NP_000834.2:p.Gln402Lys
XR_941310.1:n.1470-662G>T
NM_000843.4:c.1204C>A MANE Select	NP_000834.2:p.Gln402Lys