Canonical Allele Identifier: CA996593811
Gene: GRIN2D HGNC NCBI

Linked Data

gnomAD v3: 19-48419531-C-CTT
gnomAD v4: 19-48419531-C-CTT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419532_48419533dup , CM000681.2:g.48419532_48419533dup GRCh38
NC_000019.9:g.48922789_48922790dup , CM000681.1:g.48922789_48922790dup GRCh37
NC_000019.8:g.53614601_53614602dup NCBI36
NG_052829.1:g.29658_29659dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-53_1862-52dup MANE Select ENSP00000263269.2:n.1862-53_1862-52dup
ENST00000263269.3:c.1862-53_1862-52dup ENSP00000263269.2:n.1862-53_1862-52dup
NM_000836.2:c.1862-53_1862-52dup NP_000827.2:n.1862-53_1862-52dup
XM_011526872.1:c.1862-53_1862-52dup XP_011525174.1:n.1862-53_1862-52dup
NM_000836.4:c.1862-53_1862-52dup MANE Select NP_000827.2:n.1862-53_1862-52dup
Search 100 bp 5'
Search 100 bp 3'