Canonical Allele Identifier: CA2520897781
Gene: GRM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815444C>T , CM000669.2:g.86815444C>T GRCh38
NC_000007.13:g.86444760C>T , CM000669.1:g.86444760C>T GRCh37
NC_000007.12:g.86282696C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-23395C>T MANE Select ENSP00000355316.2:n.1325-23395C>T
ENST00000361669.6:c.1325-23395C>T ENSP00000355316.2:n.1325-23395C>T
ENST00000439827.1:c.1324+28328C>T ENSP00000398767.1:n.1324+28328C>T
NM_000840.2:c.1325-23395C>T NP_000831.2:n.1325-23395C>T
XM_011516088.1:c.1324+28328C>T XP_011514390.1:n.1324+28328C>T
XM_011516089.1:c.*197C>T XP_011514391.1:n.*197C>T
XM_011516090.1:c.1325-17578C>T XP_011514392.1:n.1325-17578C>T
NM_001363522.1:c.1324+28328C>T NP_001350451.1:n.1324+28328C>T
NM_000840.3:c.1325-23395C>T MANE Select NP_000831.2:n.1325-23395C>T
NM_001363522.2:c.1324+28328C>T NP_001350451.1:n.1324+28328C>T