Canonical Allele Identifier: CA448376192

Gene: GRM6

Linked Data

• dbSNP Id: rs1410165268
• gnomAD v4: 5-178994702-G-C
• MyVariant Identifiers: chr5:g.178421703G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.178994702G>C , CM000667.2:g.178994702G>C	GRCh38
NC_000005.9:g.178421703G>C , CM000667.1:g.178421703G>C	GRCh37
NC_000005.8:g.178354309G>C	NCBI36
NG_008105.1:g.5422C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517717.3:c.243C>G MANE Select	ENSP00000430767.1:p.Ala81=
ENST00000650031.1:c.243C>G	ENSP00000497110.1:p.Ala81=
ENST00000231188.9:c.243C>G	ENSP00000231188.5:p.Ala81=
ENST00000517717.1:c.243C>G	ENSP00000430767.1:p.Ala81=
NM_000843.3:c.243C>G	NP_000834.2:p.Ala81=
NM_000843.4:c.243C>G MANE Select	NP_000834.2:p.Ala81=