Canonical Allele Identifier: CA478853943

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.14019044_14019045insC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13866110_13866111insC , CM000674.2:g.13866110_13866111insC	GRCh38
NC_000012.11:g.14019044_14019045insC , CM000674.1:g.14019044_14019045insC	GRCh37
NC_000012.10:g.13910311_13910312insC	NCBI36
NG_031854.1:g.118978_118979insG
NG_031854.2:g.120902_120903insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.98_99insG MANE Select	ENSP00000477455.1:p.Ser34GlnfsTer25
ENST00000630791.2:c.98_99insG	ENSP00000486677.2:p.Ser34GlnfsTer25
ENST00000609686.3:c.98_99insG	ENSP00000477455.1:p.Ser34GlnfsTer25
ENST00000627535.2:c.98_99insG	ENSP00000486411.1:p.Ser34GlnfsTer?
ENST00000630791.1:c.98_99insG	ENSP00000486677.1:p.Ser34GlnfsTer?
NM_000834.3:c.98_99insG	NP_000825.2:p.Ser34GlnfsTer25
XM_011520628.1:c.98_99insG	XP_011518930.1:p.Ser34GlnfsTer25
XM_011520629.1:c.98_99insG	XP_011518931.1:p.Ser34GlnfsTer25
XM_011520630.1:c.98_99insG	XP_011518932.1:p.Ser34GlnfsTer25
NM_000834.4:c.98_99insG	NP_000825.2:p.Ser34GlnfsTer25
XM_011520628.2:c.98_99insG	XP_011518930.1:p.Ser34GlnfsTer25
XM_011520629.2:c.98_99insG	XP_011518931.1:p.Ser34GlnfsTer25
XM_017019219.2:c.98_99insG	XP_016874708.1:p.Ser34GlnfsTer25
NM_000834.5:c.98_99insG MANE Select	NP_000825.2:p.Ser34GlnfsTer25