Canonical Allele Identifier: CA203245
Gene: GRM6 HGNC NCBI

Linked Data

ClinVar Variation Id: 198107
ClinVar RCV Id: RCV000179349 RCV000625250 RCV000972586
dbSNP Id: rs5019554
ExAC: 5:178415983 G / A
gnomAD v2: 5-178415983-G-A
gnomAD v3: 5-178988982-G-A
gnomAD v4: 5-178988982-G-A
MyVariant Identifiers: chr5:g.178415983G>A (hg19) chr5:g.178988982G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178988982G>A , CM000667.2:g.178988982G>A GRCh38
NC_000005.9:g.178415983G>A , CM000667.1:g.178415983G>A GRCh37
NC_000005.8:g.178348589G>A NCBI36
NG_008105.1:g.11142C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000517717.3:c.1307C>T MANE Select ENSP00000430767.1:p.Thr436Ile
ENST00000650031.1:c.1307C>T ENSP00000497110.1:p.Thr436Ile
ENST00000231188.9:c.1307C>T ENSP00000231188.5:p.Thr436Ile
ENST00000517717.1:c.1307C>T ENSP00000430767.1:p.Thr436Ile
NM_000843.3:c.1307C>T NP_000834.2:p.Thr436Ile
XR_941310.1:n.1470-765G>A
NM_000843.4:c.1307C>T MANE Select NP_000834.2:p.Thr436Ile
Search 100 bp 5'
Search 100 bp 3'