Canonical Allele Identifier: CA448376239
Gene: GRM6 HGNC NCBI

Linked Data

dbSNP Id: rs1216564042
gnomAD v3: 5-178994767-G-A
gnomAD v4: 5-178994767-G-A
MyVariant Identifiers: chr5:g.178421768G>A (hg19) chr5:g.178994767G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994767G>A , CM000667.2:g.178994767G>A GRCh38
NC_000005.9:g.178421768G>A , CM000667.1:g.178421768G>A GRCh37
NC_000005.8:g.178354374G>A NCBI36
NG_008105.1:g.5357C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.178C>T MANE Select ENSP00000430767.1:p.Leu60=
ENST00000650031.1:c.178C>T ENSP00000497110.1:p.Leu60=
ENST00000231188.9:c.178C>T ENSP00000231188.5:p.Leu60=
ENST00000517717.1:c.178C>T ENSP00000430767.1:p.Leu60=
NM_000843.3:c.178C>T NP_000834.2:p.Leu60=
NM_000843.4:c.178C>T MANE Select NP_000834.2:p.Leu60=
Search 100 bp 5'
Search 100 bp 3'