Canonical Allele Identifier: CA2339887525

Gene: GRIN2D

Linked Data

• dbSNP Id: rs1970990154
• gnomAD v4: 19-48419508-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48419510del , CM000681.2:g.48419510del	GRCh38
NC_000019.9:g.48922767del , CM000681.1:g.48922767del	GRCh37
NC_000019.8:g.53614579del	NCBI36
NG_052829.1:g.29636del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263269.4:c.1862-75del MANE Select	ENSP00000263269.2:n.1862-75del
ENST00000263269.3:c.1862-75del	ENSP00000263269.2:n.1862-75del
NM_000836.2:c.1862-75del	NP_000827.2:n.1862-75del
XM_011526872.1:c.1862-75del	XP_011525174.1:n.1862-75del
NM_000836.4:c.1862-75del MANE Select	NP_000827.2:n.1862-75del