Canonical Allele Identifier: CA384053625
Gene: GRIN2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13865842T>A , CM000674.2:g.13865842T>A GRCh38
NC_000012.11:g.14018776T>A , CM000674.1:g.14018776T>A GRCh37
NC_000012.10:g.13910043T>A NCBI36
NG_031854.1:g.119247A>T
NG_031854.2:g.121171A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.367A>T MANE Select ENSP00000477455.1:p.Ile123Phe
ENST00000630791.2:c.367A>T ENSP00000486677.2:p.Ile123Phe
ENST00000609686.3:c.367A>T ENSP00000477455.1:p.Ile123Phe
NM_000834.3:c.367A>T NP_000825.2:p.Ile123Phe
XM_011520628.1:c.367A>T XP_011518930.1:p.Ile123Phe
XM_011520629.1:c.367A>T XP_011518931.1:p.Ile123Phe
XM_011520630.1:c.367A>T XP_011518932.1:p.Ile123Phe
NM_000834.4:c.367A>T NP_000825.2:p.Ile123Phe
XM_011520628.2:c.367A>T XP_011518930.1:p.Ile123Phe
XM_011520629.2:c.367A>T XP_011518931.1:p.Ile123Phe
XM_017019219.2:c.367A>T XP_016874708.1:p.Ile123Phe
NM_000834.5:c.367A>T MANE Select NP_000825.2:p.Ile123Phe