Canonical Allele Identifier: CA478703799

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13722771A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13569837A>G , CM000674.2:g.13569837A>G	GRCh38
NC_000012.11:g.13722771A>G , CM000674.1:g.13722771A>G	GRCh37
NC_000012.10:g.13614038A>G	NCBI36
NG_031854.1:g.415252T>C
NG_031854.2:g.417176T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.2352T>C MANE Select	ENSP00000477455.1:p.Phe784=
ENST00000628166.2:n.612T>C
ENST00000637214.1:c.69+38766T>C	ENSP00000489997.1:n.69+38766T>C
ENST00000609686.3:c.2352T>C	ENSP00000477455.1:p.Phe784=
ENST00000628166.1:n.612T>C
NM_000834.3:c.2352T>C	NP_000825.2:p.Phe784=
XM_005253351.2:c.138T>C	XP_005253408.1:p.Phe46=
XM_011520628.1:c.2352T>C	XP_011518930.1:p.Phe784=
XM_011520629.1:c.2352T>C	XP_011518931.1:p.Phe784=
XM_011520630.1:c.2352T>C	XP_011518932.1:p.Phe784=
NM_000834.4:c.2352T>C	NP_000825.2:p.Phe784=
XM_005253351.3:c.138T>C	XP_005253408.1:p.Phe46=
XM_011520628.2:c.2352T>C	XP_011518930.1:p.Phe784=
XM_011520629.2:c.2352T>C	XP_011518931.1:p.Phe784=
XM_017019219.2:c.2352T>C	XP_016874708.1:p.Phe784=
NM_000834.5:c.2352T>C MANE Select	NP_000825.2:p.Phe784=