Canonical Allele Identifier: CA2617751567

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13615456-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615460del , CM000674.2:g.13615460del	GRCh38
NC_000012.11:g.13768394del , CM000674.1:g.13768394del	GRCh37
NC_000012.10:g.13659661del	NCBI36
NG_031854.1:g.369632del
NG_031854.2:g.371556del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1500+36del MANE Select	ENSP00000477455.1:n.1500+36del
ENST00000609686.3:c.1500+36del	ENSP00000477455.1:n.1500+36del
NM_000834.3:c.1500+36del	NP_000825.2:n.1500+36del
XM_011520628.1:c.1500+36del	XP_011518930.1:n.1500+36del
XM_011520629.1:c.1500+36del	XP_011518931.1:n.1500+36del
XM_011520630.1:c.1500+36del	XP_011518932.1:n.1500+36del
XR_931372.1:n.307+234del
XR_931373.1:n.447+234del
XR_931374.1:n.246+234del
NM_000834.4:c.1500+36del	NP_000825.2:n.1500+36del
XM_011520628.2:c.1500+36del	XP_011518930.1:n.1500+36del
XM_011520629.2:c.1500+36del	XP_011518931.1:n.1500+36del
XM_017019219.2:c.1500+36del	XP_016874708.1:n.1500+36del
XR_001749013.1:n.728+234del
XR_931372.2:n.444+234del
XR_931373.2:n.586+234del
NM_000834.5:c.1500+36del MANE Select	NP_000825.2:n.1500+36del