Canonical Allele Identifier: CA996593778
Gene: GRIN2D HGNC NCBI

Linked Data

dbSNP Id: rs1970989734
gnomAD v3: 19-48419483-G-A
gnomAD v4: 19-48419483-G-A
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-102G>A MANE Select ENSP00000263269.2:n.1862-102G>A
ENST00000263269.3:c.1862-102G>A ENSP00000263269.2:n.1862-102G>A
NM_000836.2:c.1862-102G>A NP_000827.2:n.1862-102G>A
XM_011526872.1:c.1862-102G>A XP_011525174.1:n.1862-102G>A
NM_000836.4:c.1862-102G>A MANE Select NP_000827.2:n.1862-102G>A
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