Canonical Allele Identifier: CA13663072
Gene: GRIN2B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1019385

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13981909C>A , CM000674.2:g.13981909C>A GRCh38
NC_000012.11:g.14134843C>A , CM000674.1:g.14134843C>A GRCh37
NC_000012.10:g.14026110C>A NCBI36
NG_031854.1:g.3180G>T
NG_031854.2:g.5104G>T

Transcript Alleles

HGVS Amino-acid change
XM_011520629.1:c.-683+7G>T XP_011518931.1:p.=
XM_011520629.2:c.-683+7G>T
ENST00000627535.2:c.-448+7G>T ENSP00000486411.1:p.=
ENST00000630791.1:c.-683+7G>T ENSP00000486677.1:p.=