Canonical Allele Identifier: CA384050647
Gene: GRIN2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13608603C>A , CM000674.2:g.13608603C>A GRCh38
NC_000012.11:g.13761537C>A , CM000674.1:g.13761537C>A GRCh37
NC_000012.10:g.13652804C>A NCBI36
NG_031854.1:g.376486G>T
NG_031854.2:g.378410G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.2010G>T MANE Select ENSP00000477455.1:p.Lys670Asn
ENST00000628166.2:n.270G>T
ENST00000637214.1:c.69G>T ENSP00000489997.1:p.Lys23Asn
ENST00000609686.3:c.2010G>T ENSP00000477455.1:p.Lys670Asn
ENST00000628166.1:n.270G>T
NM_000834.3:c.2010G>T NP_000825.2:p.Lys670Asn
XM_005253351.2:c.-44G>T XP_005253408.1:n.-44G>T
XM_011520628.1:c.2010G>T XP_011518930.1:p.Lys670Asn
XM_011520629.1:c.2010G>T XP_011518931.1:p.Lys670Asn
XM_011520630.1:c.2010G>T XP_011518932.1:p.Lys670Asn
XR_931372.1:n.179-6495C>A
XR_931373.1:n.179-15C>A
NM_000834.4:c.2010G>T NP_000825.2:p.Lys670Asn
XM_005253351.3:c.-44G>T XP_005253408.1:n.-44G>T
XM_011520628.2:c.2010G>T XP_011518930.1:p.Lys670Asn
XM_011520629.2:c.2010G>T XP_011518931.1:p.Lys670Asn
XM_017019219.2:c.2010G>T XP_016874708.1:p.Lys670Asn
XR_001749013.1:n.318-15C>A
XR_931372.2:n.316-6495C>A
XR_931373.2:n.318-15C>A
NM_000834.5:c.2010G>T MANE Select NP_000825.2:p.Lys670Asn