Canonical Allele Identifier: CA362435833
Gene: GRM6 HGNC NCBI

Linked Data

dbSNP Id: rs1760737698

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994524G>A , CM000667.2:g.178994524G>A GRCh38
NC_000005.9:g.178421525G>A , CM000667.1:g.178421525G>A GRCh37
NC_000005.8:g.178354131G>A NCBI36
NG_008105.1:g.5600C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.421C>T MANE Select ENSP00000430767.1:p.Pro141Ser
ENST00000650031.1:c.421C>T ENSP00000497110.1:p.Pro141Ser
ENST00000231188.9:c.421C>T ENSP00000231188.5:p.Pro141Ser
ENST00000517717.1:c.421C>T ENSP00000430767.1:p.Pro141Ser
NM_000843.3:c.421C>T NP_000834.2:p.Pro141Ser
NM_000843.4:c.421C>T MANE Select NP_000834.2:p.Pro141Ser