Canonical Allele Identifier: CA2017437695
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13562476C= , CM000674.2:g.13562476C= GRCh38
NC_000012.11:g.13715410C= , CM000674.1:g.13715410C= GRCh37
NC_000012.10:g.13606677C= NCBI36
NG_031854.1:g.422613G=
NG_031854.2:g.424537G=

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.*307G= MANE Select ENSP00000477455.1:n.*307G=
ENST00000637214.1:c.69+46127G= ENSP00000489997.1:n.69+46127G=
ENST00000609686.3:c.*307G= ENSP00000477455.1:n.*307G=
NM_000834.3:c.*307G= NP_000825.2:n.*307G=
XM_005253351.2:c.*307G= XP_005253408.1:n.*307G=
XM_011520628.1:c.*307G= XP_011518930.1:n.*307G=
XM_011520629.1:c.*307G= XP_011518931.1:n.*307G=
XM_011520630.1:c.*307G= XP_011518932.1:n.*307G=
NM_000834.4:c.*307G= NP_000825.2:n.*307G=
XM_005253351.3:c.*307G= XP_005253408.1:n.*307G=
XM_011520628.2:c.*307G= XP_011518930.1:n.*307G=
XM_011520629.2:c.*307G= XP_011518931.1:n.*307G=
XM_017019219.2:c.*307G= XP_016874708.1:n.*307G=
NM_000834.5:c.*307G= MANE Select NP_000825.2:n.*307G=