Canonical Allele Identifier: CA2497029655
Gene: GRM6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178988981A= , CM000667.2:g.178988981A= GRCh38
NC_000005.9:g.178415982A= , CM000667.1:g.178415982A= GRCh37
NC_000005.8:g.178348588A= NCBI36
NG_008105.1:g.11143T=

Transcript Alleles

HGVS Amino-acid change
ENST00000517717.3:c.1308T= MANE Select ENSP00000430767.1:p.Thr436=
ENST00000650031.1:c.1308T= ENSP00000497110.1:p.Thr436=
ENST00000231188.9:c.1308T= ENSP00000231188.5:p.Thr436=
ENST00000517717.1:c.1308T= ENSP00000430767.1:p.Thr436=
NM_000843.3:c.1308T= NP_000834.2:p.Thr436=
XR_941310.1:n.1470-766A=
NM_000843.4:c.1308T= MANE Select NP_000834.2:p.Thr436=