Canonical Allele Identifier: CA2017411472
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13488772C= , CM000674.2:g.13488772C= GRCh38
NC_000012.11:g.13641706C= , CM000674.1:g.13641706C= GRCh37
NC_000012.10:g.13532973C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000637214.1:c.70-50761G= ENSP00000489997.1:n.70-50761G=