Canonical Allele Identifier: CA384050916

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13761595G>C (hg19) ; chr12:g.13608661G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608661G>C , CM000674.2:g.13608661G>C	GRCh38
NC_000012.11:g.13761595G>C , CM000674.1:g.13761595G>C	GRCh37
NC_000012.10:g.13652862G>C	NCBI36
NG_031854.1:g.376428C>G
NG_031854.2:g.378352C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1952C>G MANE Select	ENSP00000477455.1:p.Ala651Gly
ENST00000628166.2:n.212C>G
ENST00000637214.1:c.11C>G	ENSP00000489997.1:p.Ala4Gly
ENST00000609686.3:c.1952C>G	ENSP00000477455.1:p.Ala651Gly
ENST00000628166.1:n.212C>G
NM_000834.3:c.1952C>G	NP_000825.2:p.Ala651Gly
XM_005253351.2:c.-102C>G	XP_005253408.1:n.-102C>G
XM_011520628.1:c.1952C>G	XP_011518930.1:p.Ala651Gly
XM_011520629.1:c.1952C>G	XP_011518931.1:p.Ala651Gly
XM_011520630.1:c.1952C>G	XP_011518932.1:p.Ala651Gly
XR_931372.1:n.179-6437G>C
XR_931373.1:n.222G>C
NM_000834.4:c.1952C>G	NP_000825.2:p.Ala651Gly
XM_005253351.3:c.-102C>G	XP_005253408.1:n.-102C>G
XM_011520628.2:c.1952C>G	XP_011518930.1:p.Ala651Gly
XM_011520629.2:c.1952C>G	XP_011518931.1:p.Ala651Gly
XM_017019219.2:c.1952C>G	XP_016874708.1:p.Ala651Gly
XR_001749013.1:n.361G>C
XR_931372.2:n.316-6437G>C
XR_931373.2:n.361G>C
NM_000834.5:c.1952C>G MANE Select	NP_000825.2:p.Ala651Gly