Canonical Allele Identifier: CA996593818
Gene: GRIN2D HGNC NCBI

Linked Data

gnomAD v3: 19-48419541-G-T
gnomAD v4: 19-48419541-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419541G>T , CM000681.2:g.48419541G>T GRCh38
NC_000019.9:g.48922798G>T , CM000681.1:g.48922798G>T GRCh37
NC_000019.8:g.53614610G>T NCBI36
NG_052829.1:g.29667G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-44G>T MANE Select ENSP00000263269.2:n.1862-44G>T
ENST00000263269.3:c.1862-44G>T ENSP00000263269.2:n.1862-44G>T
NM_000836.2:c.1862-44G>T NP_000827.2:n.1862-44G>T
XM_011526872.1:c.1862-44G>T XP_011525174.1:n.1862-44G>T
NM_000836.4:c.1862-44G>T MANE Select NP_000827.2:n.1862-44G>T
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