Canonical Allele Identifier: CA448027924
Gene: GRM6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.178421568C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994567C>A , CM000667.2:g.178994567C>A GRCh38
NC_000005.9:g.178421568C>A , CM000667.1:g.178421568C>A GRCh37
NC_000005.8:g.178354174C>A NCBI36
NG_008105.1:g.5557G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.378G>T MANE Select ENSP00000430767.1:p.Val126=
ENST00000650031.1:c.378G>T ENSP00000497110.1:p.Val126=
ENST00000231188.9:c.378G>T ENSP00000231188.5:p.Val126=
ENST00000517717.1:c.378G>T ENSP00000430767.1:p.Val126=
NM_000843.3:c.378G>T NP_000834.2:p.Val126=
NM_000843.4:c.378G>T MANE Select NP_000834.2:p.Val126=