Canonical Allele Identifier: CA1723229475
Gene: GRM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86644771G= , CM000669.2:g.86644771G= GRCh38
NC_000007.13:g.86274087G= , CM000669.1:g.86274087G= GRCh37
NC_000007.12:g.86112023G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_000840.3:c.-242G= MANE Select NP_000831.2:n.-242G=
ENST00000361669.7:c.-242G= MANE Select ENSP00000355316.2:n.-242G=
NM_000840.2:c.-242G= NP_000831.2:n.-242G=
NM_001363522.1:c.-242G= NP_001350451.1:n.-242G=
NM_001363522.2:c.-242G= NP_001350451.1:n.-242G=
ENST00000361669.6:c.-242G= ENSP00000355316.2:n.-242G=
ENST00000454217.1:c.-18G= ENSP00000405427.1:n.-18G=
XM_011516088.1:c.-242G= XP_011514390.1:n.-242G=
XM_011516089.1:c.-242G= XP_011514391.1:n.-242G=
XM_011516090.1:c.-242G= XP_011514392.1:n.-242G=
XM_017012073.2:c.-242G= XP_016867562.1:n.-242G=