Canonical Allele Identifier: CA508038073
Gene: GRIN2D HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.48922867T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419610T>A , CM000681.2:g.48419610T>A GRCh38
NC_000019.9:g.48922867T>A , CM000681.1:g.48922867T>A GRCh37
NC_000019.8:g.53614679T>A NCBI36
NG_052829.1:g.29736T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1887T>A MANE Select ENSP00000263269.2:p.Ile629=
ENST00000263269.3:c.1887T>A ENSP00000263269.2:p.Ile629=
NM_000836.2:c.1887T>A NP_000827.2:p.Ile629=
XM_011526872.1:c.1887T>A XP_011525174.1:p.Ile629=
NM_000836.4:c.1887T>A MANE Select NP_000827.2:p.Ile629=
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