Canonical Allele Identifier: CA2017578271
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13866115G= , CM000674.2:g.13866115G= GRCh38
NC_000012.11:g.14019049G= , CM000674.1:g.14019049G= GRCh37
NC_000012.10:g.13910316G= NCBI36
NG_031854.1:g.118974C=
NG_031854.2:g.120898C=

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.94C= MANE Select ENSP00000477455.1:p.Pro32=
ENST00000630791.2:c.94C= ENSP00000486677.2:p.Pro32=
ENST00000609686.3:c.94C= ENSP00000477455.1:p.Pro32=
ENST00000627535.2:c.94C= ENSP00000486411.1:p.Pro32=
ENST00000630791.1:c.94C= ENSP00000486677.1:p.Pro32=
NM_000834.3:c.94C= NP_000825.2:p.Pro32=
XM_011520628.1:c.94C= XP_011518930.1:p.Pro32=
XM_011520629.1:c.94C= XP_011518931.1:p.Pro32=
XM_011520630.1:c.94C= XP_011518932.1:p.Pro32=
NM_000834.4:c.94C= NP_000825.2:p.Pro32=
XM_011520628.2:c.94C= XP_011518930.1:p.Pro32=
XM_011520629.2:c.94C= XP_011518931.1:p.Pro32=
XM_017019219.2:c.94C= XP_016874708.1:p.Pro32=
NM_000834.5:c.94C= MANE Select NP_000825.2:p.Pro32=