Canonical Allele Identifier: CA2339887511
Gene: GRIN2D HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419483G= , CM000681.2:g.48419483G= GRCh38
NC_000019.9:g.48922740G= , CM000681.1:g.48922740G= GRCh37
NC_000019.8:g.53614552G= NCBI36
NG_052829.1:g.29609G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-102G= MANE Select ENSP00000263269.2:n.1862-102G=
ENST00000263269.3:c.1862-102G= ENSP00000263269.2:n.1862-102G=
NM_000836.2:c.1862-102G= NP_000827.2:n.1862-102G=
XM_011526872.1:c.1862-102G= XP_011525174.1:n.1862-102G=
NM_000836.4:c.1862-102G= MANE Select NP_000827.2:n.1862-102G=
Search 100 bp 5'
Search 100 bp 3'