Canonical Allele Identifier: CA448027889

Gene: GRM6

Linked Data

• MyVariant Identifiers: chr5:g.178421535C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.178994534C>G , CM000667.2:g.178994534C>G	GRCh38
NC_000005.9:g.178421535C>G , CM000667.1:g.178421535C>G	GRCh37
NC_000005.8:g.178354141C>G	NCBI36
NG_008105.1:g.5590G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517717.3:c.411G>C MANE Select	ENSP00000430767.1:p.Leu137=
ENST00000650031.1:c.411G>C	ENSP00000497110.1:p.Leu137=
ENST00000231188.9:c.411G>C	ENSP00000231188.5:p.Leu137=
ENST00000517717.1:c.411G>C	ENSP00000430767.1:p.Leu137=
NM_000843.3:c.411G>C	NP_000834.2:p.Leu137=
NM_000843.4:c.411G>C MANE Select	NP_000834.2:p.Leu137=