Canonical Allele Identifier: CA448375658
Gene: GRM6 HGNC NCBI

Linked Data

COSMIC: COSM161422
MyVariant Identifiers: chr5:g.178416090C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178989089C>T , CM000667.2:g.178989089C>T GRCh38
NC_000005.9:g.178416090C>T , CM000667.1:g.178416090C>T GRCh37
NC_000005.8:g.178348696C>T NCBI36
NG_008105.1:g.11035G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.1200G>A MANE Select ENSP00000430767.1:p.Lys400=
ENST00000650031.1:c.1200G>A ENSP00000497110.1:p.Lys400=
ENST00000231188.9:c.1200G>A ENSP00000231188.5:p.Lys400=
ENST00000517717.1:c.1200G>A ENSP00000430767.1:p.Lys400=
NM_000843.3:c.1200G>A NP_000834.2:p.Lys400=
XR_941310.1:n.1470-658C>T
NM_000843.4:c.1200G>A MANE Select NP_000834.2:p.Lys400=