Canonical Allele Identifier: CA448027891
Gene: GRM6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1146605
ClinVar RCV Id: RCV001485898
dbSNP Id: rs2113347613
gnomAD v4: 5-178994536-G-A
MyVariant Identifiers: chr5:g.178421537G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994536G>A , CM000667.2:g.178994536G>A GRCh38
NC_000005.9:g.178421537G>A , CM000667.1:g.178421537G>A GRCh37
NC_000005.8:g.178354143G>A NCBI36
NG_008105.1:g.5588C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.409C>T MANE Select ENSP00000430767.1:p.Leu137=
ENST00000650031.1:c.409C>T ENSP00000497110.1:p.Leu137=
ENST00000231188.9:c.409C>T ENSP00000231188.5:p.Leu137=
ENST00000517717.1:c.409C>T ENSP00000430767.1:p.Leu137=
NM_000843.3:c.409C>T NP_000834.2:p.Leu137=
NM_000843.4:c.409C>T MANE Select NP_000834.2:p.Leu137=
Search 100 bp 5'
Search 100 bp 3'