Canonical Allele Identifier: CA478772825

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13768157G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615223G>A , CM000674.2:g.13615223G>A	GRCh38
NC_000012.11:g.13768157G>A , CM000674.1:g.13768157G>A	GRCh37
NC_000012.10:g.13659424G>A	NCBI36
NG_031854.1:g.369866C>T
NG_031854.2:g.371790C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1545C>T MANE Select	ENSP00000477455.1:p.Ile515=
ENST00000609686.3:c.1545C>T	ENSP00000477455.1:p.Ile515=
NM_000834.3:c.1545C>T	NP_000825.2:p.Ile515=
XM_011520628.1:c.1545C>T	XP_011518930.1:p.Ile515=
XM_011520629.1:c.1545C>T	XP_011518931.1:p.Ile515=
XM_011520630.1:c.1545C>T	XP_011518932.1:p.Ile515=
XR_931372.1:n.304G>A
XR_931373.1:n.444G>A
XR_931374.1:n.243G>A
NM_000834.4:c.1545C>T	NP_000825.2:p.Ile515=
XM_011520628.2:c.1545C>T	XP_011518930.1:p.Ile515=
XM_011520629.2:c.1545C>T	XP_011518931.1:p.Ile515=
XM_017019219.2:c.1545C>T	XP_016874708.1:p.Ile515=
XR_001749013.1:n.725G>A
XR_931372.2:n.441G>A
XR_931373.2:n.583G>A
NM_000834.5:c.1545C>T MANE Select	NP_000825.2:p.Ile515=