Canonical Allele Identifier: CA362429946

Gene: GRM6

Linked Data

• gnomAD v4: 5-178988982-G-C
• MyVariant Identifiers: chr5:g.178415983G>C (hg19) ; chr5:g.178988982G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.178988982G>C , CM000667.2:g.178988982G>C	GRCh38
NC_000005.9:g.178415983G>C , CM000667.1:g.178415983G>C	GRCh37
NC_000005.8:g.178348589G>C	NCBI36
NG_008105.1:g.11142C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517717.3:c.1307C>G MANE Select	ENSP00000430767.1:p.Thr436Ser
ENST00000650031.1:c.1307C>G	ENSP00000497110.1:p.Thr436Ser
ENST00000231188.9:c.1307C>G	ENSP00000231188.5:p.Thr436Ser
ENST00000517717.1:c.1307C>G	ENSP00000430767.1:p.Thr436Ser
NM_000843.3:c.1307C>G	NP_000834.2:p.Thr436Ser
XR_941310.1:n.1470-765G>C
NM_000843.4:c.1307C>G MANE Select	NP_000834.2:p.Thr436Ser