Canonical Allele Identifier: CA362436116
Gene: GRM6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.178421593C>G (hg19) chr5:g.178994592C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994592C>G , CM000667.2:g.178994592C>G GRCh38
NC_000005.9:g.178421593C>G , CM000667.1:g.178421593C>G GRCh37
NC_000005.8:g.178354199C>G NCBI36
NG_008105.1:g.5532G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.353G>C MANE Select ENSP00000430767.1:p.Arg118Pro
ENST00000650031.1:c.353G>C ENSP00000497110.1:p.Arg118Pro
ENST00000231188.9:c.353G>C ENSP00000231188.5:p.Arg118Pro
ENST00000517717.1:c.353G>C ENSP00000430767.1:p.Arg118Pro
NM_000843.3:c.353G>C NP_000834.2:p.Arg118Pro
NM_000843.4:c.353G>C MANE Select NP_000834.2:p.Arg118Pro
Search 100 bp 5'
Search 100 bp 3'