Canonical Allele Identifier: CA2617751487

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13615384-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615384G>A , CM000674.2:g.13615384G>A	GRCh38
NC_000012.11:g.13768318G>A , CM000674.1:g.13768318G>A	GRCh37
NC_000012.10:g.13659585G>A	NCBI36
NG_031854.1:g.369705C>T
NG_031854.2:g.371629C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1500+109C>T MANE Select	ENSP00000477455.1:n.1500+109C>T
ENST00000609686.3:c.1500+109C>T	ENSP00000477455.1:n.1500+109C>T
NM_000834.3:c.1500+109C>T	NP_000825.2:n.1500+109C>T
XM_011520628.1:c.1500+109C>T	XP_011518930.1:n.1500+109C>T
XM_011520629.1:c.1500+109C>T	XP_011518931.1:n.1500+109C>T
XM_011520630.1:c.1500+109C>T	XP_011518932.1:n.1500+109C>T
XR_931372.1:n.307+158G>A
XR_931373.1:n.447+158G>A
XR_931374.1:n.246+158G>A
NM_000834.4:c.1500+109C>T	NP_000825.2:n.1500+109C>T
XM_011520628.2:c.1500+109C>T	XP_011518930.1:n.1500+109C>T
XM_011520629.2:c.1500+109C>T	XP_011518931.1:n.1500+109C>T
XM_017019219.2:c.1500+109C>T	XP_016874708.1:n.1500+109C>T
XR_001749013.1:n.728+158G>A
XR_931372.2:n.444+158G>A
XR_931373.2:n.586+158G>A
NM_000834.5:c.1500+109C>T MANE Select	NP_000825.2:n.1500+109C>T