Canonical Allele Identifier: CA3594131
Gene: GRM6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1419110
ClinVar RCV Id: RCV001940590
dbSNP Id: rs200167284
ExAC: 5:178415987 G / A
gnomAD v2: 5-178415987-G-A
gnomAD v3: 5-178988986-G-A
gnomAD v4: 5-178988986-G-A
MyVariant Identifiers: chr5:g.178415987G>A (hg19) chr5:g.178988986G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178988986G>A , CM000667.2:g.178988986G>A GRCh38
NC_000005.9:g.178415987G>A , CM000667.1:g.178415987G>A GRCh37
NC_000005.8:g.178348593G>A NCBI36
NG_008105.1:g.11138C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.1303C>T MANE Select ENSP00000430767.1:p.Pro435Ser
ENST00000650031.1:c.1303C>T ENSP00000497110.1:p.Pro435Ser
ENST00000231188.9:c.1303C>T ENSP00000231188.5:p.Pro435Ser
ENST00000517717.1:c.1303C>T ENSP00000430767.1:p.Pro435Ser
NM_000843.3:c.1303C>T NP_000834.2:p.Pro435Ser
XR_941310.1:n.1470-761G>A
NM_000843.4:c.1303C>T MANE Select NP_000834.2:p.Pro435Ser
Search 100 bp 5'
Search 100 bp 3'