Canonical Allele Identifier: CA13720689
Gene: GRIN2B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4764043

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13962548C>T , CM000674.2:g.13962548C>T GRCh38
NC_000012.11:g.14115482C>T , CM000674.1:g.14115482C>T GRCh37
NC_000012.10:g.14006749C>T NCBI36
NG_031854.1:g.22541G>A
NG_031854.2:g.24465G>A

Transcript Alleles

HGVS Amino-acid change
NM_000834.3:c.-19+17380G>A VV NP_000825.2:p.=
XM_011520628.1:c.-19+17380G>A XP_011518930.1:p.=
XM_011520629.1:c.-19+17380G>A XP_011518931.1:p.=
XM_011520630.1:c.-19+17380G>A XP_011518932.1:p.=
NM_000834.4:c.-19+17380G>A VV NP_000825.2:p.=
XM_011520628.2:c.-19+17380G>A XP_011518930.1:p.=
XM_011520629.2:c.-19+17380G>A XP_011518931.1:p.=
XM_017019219.2:c.-19+17380G>A XP_016874708.1:p.=
ENST00000609686.3:c.-19+17380G>A ENSP00000477455.1:p.=
ENST00000627535.2:c.-19+17380G>A ENSP00000486411.1:p.=
ENST00000630791.1:c.-19+17380G>A ENSP00000486677.1:p.=