Canonical Allele Identifier: CA1723318396
Gene: GRM3 HGNC NCBI

Linked Data

dbSNP Id: rs1798006671

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815970A>G , CM000669.2:g.86815970A>G GRCh38
NC_000007.13:g.86445286A>G , CM000669.1:g.86445286A>G GRCh37
NC_000007.12:g.86283222A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-22869A>G MANE Select ENSP00000355316.2:n.1325-22869A>G
ENST00000361669.6:c.1325-22869A>G ENSP00000355316.2:n.1325-22869A>G
ENST00000439827.1:c.1324+28854A>G ENSP00000398767.1:n.1324+28854A>G
NM_000840.2:c.1325-22869A>G NP_000831.2:n.1325-22869A>G
XM_011516088.1:c.1324+28854A>G XP_011514390.1:n.1324+28854A>G
XM_011516090.1:c.1325-17052A>G XP_011514392.1:n.1325-17052A>G
NM_001363522.1:c.1324+28854A>G NP_001350451.1:n.1324+28854A>G
NM_000840.3:c.1325-22869A>G MANE Select NP_000831.2:n.1325-22869A>G
NM_001363522.2:c.1324+28854A>G NP_001350451.1:n.1324+28854A>G