Canonical Allele Identifier: CA362437017
Gene: GRM6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2415551
ClinVar RCV Id: RCV003104763
dbSNP Id: rs1211186758
gnomAD v2: 5-178421819-C-A
gnomAD v3: 5-178994818-C-A
gnomAD v4: 5-178994818-C-A
MyVariant Identifiers: chr5:g.178421819C>A (hg19) chr5:g.178994818C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994818C>A , CM000667.2:g.178994818C>A GRCh38
NC_000005.9:g.178421819C>A , CM000667.1:g.178421819C>A GRCh37
NC_000005.8:g.178354425C>A NCBI36
NG_008105.1:g.5306G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.127G>T MANE Select ENSP00000430767.1:p.Gly43Cys
ENST00000650031.1:c.127G>T ENSP00000497110.1:p.Gly43Cys
ENST00000231188.9:c.127G>T ENSP00000231188.5:p.Gly43Cys
ENST00000517717.1:c.127G>T ENSP00000430767.1:p.Gly43Cys
NM_000843.3:c.127G>T NP_000834.2:p.Gly43Cys
NM_000843.4:c.127G>T MANE Select NP_000834.2:p.Gly43Cys
Search 100 bp 5'
Search 100 bp 3'