Canonical Allele Identifier: CA448376292
Gene: GRM6 HGNC NCBI

Linked Data

gnomAD v4: 5-178994813-C-G
MyVariant Identifiers: chr5:g.178421814C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994813C>G , CM000667.2:g.178994813C>G GRCh38
NC_000005.9:g.178421814C>G , CM000667.1:g.178421814C>G GRCh37
NC_000005.8:g.178354420C>G NCBI36
NG_008105.1:g.5311G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.132G>C MANE Select ENSP00000430767.1:p.Leu44=
ENST00000650031.1:c.132G>C ENSP00000497110.1:p.Leu44=
ENST00000231188.9:c.132G>C ENSP00000231188.5:p.Leu44=
ENST00000517717.1:c.132G>C ENSP00000430767.1:p.Leu44=
NM_000843.3:c.132G>C NP_000834.2:p.Leu44=
NM_000843.4:c.132G>C MANE Select NP_000834.2:p.Leu44=
Search 100 bp 5'
Search 100 bp 3'