Canonical Allele Identifier: CA2617751132

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13615066-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615070del , CM000674.2:g.13615070del	GRCh38
NC_000012.11:g.13768004del , CM000674.1:g.13768004del	GRCh37
NC_000012.10:g.13659271del	NCBI36
NG_031854.1:g.370022del
NG_031854.2:g.371946del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1654+47del MANE Select	ENSP00000477455.1:n.1654+47del
ENST00000609686.3:c.1654+47del	ENSP00000477455.1:n.1654+47del
NM_000834.3:c.1654+47del	NP_000825.2:n.1654+47del
XM_011520628.1:c.1654+47del	XP_011518930.1:n.1654+47del
XM_011520629.1:c.1654+47del	XP_011518931.1:n.1654+47del
XM_011520630.1:c.1654+47del	XP_011518932.1:n.1654+47del
XR_931372.1:n.179-28del
XR_931373.1:n.319-28del
XR_931374.1:n.118-28del
NM_000834.4:c.1654+47del	NP_000825.2:n.1654+47del
XM_011520628.2:c.1654+47del	XP_011518930.1:n.1654+47del
XM_011520629.2:c.1654+47del	XP_011518931.1:n.1654+47del
XM_017019219.2:c.1654+47del	XP_016874708.1:n.1654+47del
XR_001749013.1:n.600-28del
XR_931372.2:n.316-28del
XR_931373.2:n.458-28del
NM_000834.5:c.1654+47del MANE Select	NP_000825.2:n.1654+47del