Canonical Allele Identifier: CA233132067
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs866527616

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13562381G>A , CM000674.2:g.13562381G>A GRCh38
NC_000012.11:g.13715315G>A , CM000674.1:g.13715315G>A GRCh37
NC_000012.10:g.13606582G>A NCBI36
NG_031854.1:g.422708C>T
NG_031854.2:g.424632C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.*402C>T MANE Select ENSP00000477455.1:n.*402C>T
ENST00000637214.1:c.69+46222C>T ENSP00000489997.1:n.69+46222C>T
ENST00000609686.3:c.*402C>T ENSP00000477455.1:n.*402C>T
NM_000834.3:c.*402C>T NP_000825.2:n.*402C>T
XM_005253351.2:c.*402C>T XP_005253408.1:n.*402C>T
XM_011520628.1:c.*402C>T XP_011518930.1:n.*402C>T
XM_011520629.1:c.*402C>T XP_011518931.1:n.*402C>T
XM_011520630.1:c.*402C>T XP_011518932.1:n.*402C>T
NM_000834.4:c.*402C>T NP_000825.2:n.*402C>T
XM_005253351.3:c.*402C>T XP_005253408.1:n.*402C>T
XM_011520628.2:c.*402C>T XP_011518930.1:n.*402C>T
XM_011520629.2:c.*402C>T XP_011518931.1:n.*402C>T
XM_017019219.2:c.*402C>T XP_016874708.1:n.*402C>T
NM_000834.5:c.*402C>T MANE Select NP_000825.2:n.*402C>T