Canonical Allele Identifier: CA2617752992

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13608900-ACACAGGGTGAGTC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608902_13608914del , CM000674.2:g.13608902_13608914del	GRCh38
NC_000012.11:g.13761836_13761848del , CM000674.1:g.13761836_13761848del	GRCh37
NC_000012.10:g.13653103_13653115del	NCBI36
NG_031854.1:g.376176_376188del
NG_031854.2:g.378100_378112del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1781-81_1781-69del MANE Select	ENSP00000477455.1:n.1781-81_1781-69del
ENST00000628166.2:n.41-81_41-69del
ENST00000609686.3:c.1781-81_1781-69del	ENSP00000477455.1:n.1781-81_1781-69del
ENST00000628166.1:n.41-81_41-69del
NM_000834.3:c.1781-81_1781-69del	NP_000825.2:n.1781-81_1781-69del
XM_011520628.1:c.1781-81_1781-69del	XP_011518930.1:n.1781-81_1781-69del
XM_011520629.1:c.1781-81_1781-69del	XP_011518931.1:n.1781-81_1781-69del
XM_011520630.1:c.1781-81_1781-69del	XP_011518932.1:n.1781-81_1781-69del
XR_931372.1:n.179-6196_179-6184del
XR_931373.1:n.318+145_318+157del
NM_000834.4:c.1781-81_1781-69del	NP_000825.2:n.1781-81_1781-69del
XM_011520628.2:c.1781-81_1781-69del	XP_011518930.1:n.1781-81_1781-69del
XM_011520629.2:c.1781-81_1781-69del	XP_011518931.1:n.1781-81_1781-69del
XM_017019219.2:c.1781-81_1781-69del	XP_016874708.1:n.1781-81_1781-69del
XR_001749013.1:n.457+145_457+157del
XR_931372.2:n.316-6196_316-6184del
XR_931373.2:n.457+145_457+157del
NM_000834.5:c.1781-81_1781-69del MANE Select	NP_000825.2:n.1781-81_1781-69del