Canonical Allele Identifier: CA362437192
Gene: GRM6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1391424
ClinVar RCV Id: RCV001910992
dbSNP Id: rs1760747050
gnomAD v4: 5-178994907-A-G
MyVariant Identifiers: chr5:g.178421908A>G (hg19) chr5:g.178994907A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994907A>G , CM000667.2:g.178994907A>G GRCh38
NC_000005.9:g.178421908A>G , CM000667.1:g.178421908A>G GRCh37
NC_000005.8:g.178354514A>G NCBI36
NG_008105.1:g.5217T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.38T>C MANE Select ENSP00000430767.1:p.Val13Ala
ENST00000650031.1:c.38T>C ENSP00000497110.1:p.Val13Ala
ENST00000231188.9:c.38T>C ENSP00000231188.5:p.Val13Ala
ENST00000517717.1:c.38T>C ENSP00000430767.1:p.Val13Ala
NM_000843.3:c.38T>C NP_000834.2:p.Val13Ala
NM_000843.4:c.38T>C MANE Select NP_000834.2:p.Val13Ala
Search 100 bp 5'
Search 100 bp 3'