Canonical Allele Identifier: CA133035581

Gene: GRM6

Linked Data

• dbSNP Id: rs868030567
• gnomAD v2: 5-178422013-C-G
• gnomAD v3: 5-178995012-C-G
• gnomAD v4: 5-178995012-C-G
• MyVariant Identifiers: chr5:g.178422013C>G (hg19) ; chr5:g.178995012C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.178995012C>G , CM000667.2:g.178995012C>G	GRCh38
NC_000005.9:g.178422013C>G , CM000667.1:g.178422013C>G	GRCh37
NC_000005.8:g.178354619C>G	NCBI36
NG_008105.1:g.5112G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517717.3:c.-16-52G>C MANE Select	ENSP00000430767.1:n.-16-52G>C
ENST00000650031.1:c.-16-52G>C	ENSP00000497110.1:n.-16-52G>C
ENST00000231188.9:c.-68G>C	ENSP00000231188.5:n.-68G>C
ENST00000517717.1:c.-16-52G>C	ENSP00000430767.1:n.-16-52G>C
NM_000843.3:c.-68G>C	NP_000834.2:n.-68G>C
NM_000843.4:c.-16-52G>C MANE Select	NP_000834.2:n.-16-52G>C