Canonical Allele Identifier: CA2017510041
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13719075T= , CM000674.2:g.13719075T= GRCh38
NC_000012.11:g.13872009T= , CM000674.1:g.13872009T= GRCh37
NC_000012.10:g.13763276T= NCBI36
NG_031854.1:g.266014A=
NG_031854.2:g.267938A=

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.1010+34242A= MANE Select ENSP00000477455.1:n.1010+34242A=
ENST00000630791.2:c.1010+34242A= ENSP00000486677.2:n.1010+34242A=
ENST00000609686.3:c.1010+34242A= ENSP00000477455.1:n.1010+34242A=
NM_000834.3:c.1010+34242A= NP_000825.2:n.1010+34242A=
XM_011520628.1:c.1010+34242A= XP_011518930.1:n.1010+34242A=
XM_011520629.1:c.1010+34242A= XP_011518931.1:n.1010+34242A=
XM_011520630.1:c.1010+34242A= XP_011518932.1:n.1010+34242A=
NM_000834.4:c.1010+34242A= NP_000825.2:n.1010+34242A=
XM_011520628.2:c.1010+34242A= XP_011518930.1:n.1010+34242A=
XM_011520629.2:c.1010+34242A= XP_011518931.1:n.1010+34242A=
XM_017019219.2:c.1010+34242A= XP_016874708.1:n.1010+34242A=
NM_000834.5:c.1010+34242A= MANE Select NP_000825.2:n.1010+34242A=