Canonical Allele Identifier: CA384055144

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1164700607
• gnomAD v2: 12-14019115-G-A
• gnomAD v4: 12-13866181-G-A
• MyVariant Identifiers: chr12:g.14019115G>A (hg19) ; chr12:g.13866181G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13866181G>A , CM000674.2:g.13866181G>A	GRCh38
NC_000012.11:g.14019115G>A , CM000674.1:g.14019115G>A	GRCh37
NC_000012.10:g.13910382G>A	NCBI36
NG_031854.1:g.118908C>T
NG_031854.2:g.120832C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.28C>T MANE Select	ENSP00000477455.1:p.Pro10Ser
ENST00000630791.2:c.28C>T	ENSP00000486677.2:p.Pro10Ser
ENST00000609686.3:c.28C>T	ENSP00000477455.1:p.Pro10Ser
ENST00000627535.2:c.28C>T	ENSP00000486411.1:p.Pro10Ser
ENST00000630791.1:c.28C>T	ENSP00000486677.1:p.Pro10Ser
NM_000834.3:c.28C>T	NP_000825.2:p.Pro10Ser
XM_011520628.1:c.28C>T	XP_011518930.1:p.Pro10Ser
XM_011520629.1:c.28C>T	XP_011518931.1:p.Pro10Ser
XM_011520630.1:c.28C>T	XP_011518932.1:p.Pro10Ser
NM_000834.4:c.28C>T	NP_000825.2:p.Pro10Ser
XM_011520628.2:c.28C>T	XP_011518930.1:p.Pro10Ser
XM_011520629.2:c.28C>T	XP_011518931.1:p.Pro10Ser
XM_017019219.2:c.28C>T	XP_016874708.1:p.Pro10Ser
NM_000834.5:c.28C>T MANE Select	NP_000825.2:p.Pro10Ser