Canonical Allele Identifier: CA362435790
Gene: GRM6 HGNC NCBI

Linked Data

dbSNP Id: rs1760737378
gnomAD v4: 5-178994512-C-A
MyVariant Identifiers: chr5:g.178421513C>A (hg19) chr5:g.178994512C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994512C>A , CM000667.2:g.178994512C>A GRCh38
NC_000005.9:g.178421513C>A , CM000667.1:g.178421513C>A GRCh37
NC_000005.8:g.178354119C>A NCBI36
NG_008105.1:g.5612G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.433G>T MANE Select ENSP00000430767.1:p.Val145Phe
ENST00000650031.1:c.433G>T ENSP00000497110.1:p.Val145Phe
ENST00000231188.9:c.433G>T ENSP00000231188.5:p.Val145Phe
ENST00000517717.1:c.433G>T ENSP00000430767.1:p.Val145Phe
NM_000843.3:c.433G>T NP_000834.2:p.Val145Phe
NM_000843.4:c.433G>T MANE Select NP_000834.2:p.Val145Phe
Search 100 bp 5'
Search 100 bp 3'