Canonical Allele Identifier: CA2844618254
Gene: GRM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815615G>C , CM000669.2:g.86815615G>C GRCh38
NC_000007.13:g.86444931G>C , CM000669.1:g.86444931G>C GRCh37
NC_000007.12:g.86282867G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-23224G>C MANE Select ENSP00000355316.2:n.1325-23224G>C
ENST00000361669.6:c.1325-23224G>C ENSP00000355316.2:n.1325-23224G>C
ENST00000439827.1:c.1324+28499G>C ENSP00000398767.1:n.1324+28499G>C
NM_000840.2:c.1325-23224G>C NP_000831.2:n.1325-23224G>C
XM_011516088.1:c.1324+28499G>C XP_011514390.1:n.1324+28499G>C
XM_011516090.1:c.1325-17407G>C XP_011514392.1:n.1325-17407G>C
NM_001363522.1:c.1324+28499G>C NP_001350451.1:n.1324+28499G>C
NM_000840.3:c.1325-23224G>C MANE Select NP_000831.2:n.1325-23224G>C
NM_001363522.2:c.1324+28499G>C NP_001350451.1:n.1324+28499G>C