Canonical Allele Identifier: CA448375656
Gene: GRM6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.178416087C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178989086C>G , CM000667.2:g.178989086C>G GRCh38
NC_000005.9:g.178416087C>G , CM000667.1:g.178416087C>G GRCh37
NC_000005.8:g.178348693C>G NCBI36
NG_008105.1:g.11038G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.1203G>C MANE Select ENSP00000430767.1:p.Val401=
ENST00000650031.1:c.1203G>C ENSP00000497110.1:p.Val401=
ENST00000231188.9:c.1203G>C ENSP00000231188.5:p.Val401=
ENST00000517717.1:c.1203G>C ENSP00000430767.1:p.Val401=
NM_000843.3:c.1203G>C NP_000834.2:p.Val401=
XR_941310.1:n.1470-661C>G
NM_000843.4:c.1203G>C MANE Select NP_000834.2:p.Val401=