Canonical Allele Identifier: CA448375652

Gene: GRM6

Linked Data

• MyVariant Identifiers: chr5:g.178416078C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.178989077C>A , CM000667.2:g.178989077C>A	GRCh38
NC_000005.9:g.178416078C>A , CM000667.1:g.178416078C>A	GRCh37
NC_000005.8:g.178348684C>A	NCBI36
NG_008105.1:g.11047G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000517717.3:c.1212G>T MANE Select	ENSP00000430767.1:p.Val404=
ENST00000650031.1:c.1212G>T	ENSP00000497110.1:p.Val404=
ENST00000231188.9:c.1212G>T	ENSP00000231188.5:p.Val404=
ENST00000517717.1:c.1212G>T	ENSP00000430767.1:p.Val404=
NM_000843.3:c.1212G>T	NP_000834.2:p.Val404=
XR_941310.1:n.1470-670C>A
NM_000843.4:c.1212G>T MANE Select	NP_000834.2:p.Val404=