Canonical Allele Identifier: CA233159107

Gene: GRIN2B

Linked Data

• dbSNP Id: rs752370604
• gnomAD v3: 12-13962496-T-G
• gnomAD v4: 12-13962496-T-G
• MyVariant Identifiers: chr12:g.14115430T>G (hg19) ; chr12:g.13962496T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13962496T>G , CM000674.2:g.13962496T>G	GRCh38
NC_000012.11:g.14115430T>G , CM000674.1:g.14115430T>G	GRCh37
NC_000012.10:g.14006697T>G	NCBI36
NG_031854.1:g.22593A>C
NG_031854.2:g.24517A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.-19+17432A>C MANE Select	ENSP00000477455.1:n.-19+17432A>C
ENST00000630791.2:c.-19+17432A>C	ENSP00000486677.2:n.-19+17432A>C
ENST00000609686.3:c.-19+17432A>C	ENSP00000477455.1:n.-19+17432A>C
ENST00000627535.2:c.-19+17432A>C	ENSP00000486411.1:n.-19+17432A>C
ENST00000630791.1:c.-19+17432A>C	ENSP00000486677.1:n.-19+17432A>C
NM_000834.3:c.-19+17432A>C	NP_000825.2:n.-19+17432A>C
XM_011520628.1:c.-19+17432A>C	XP_011518930.1:n.-19+17432A>C
XM_011520629.1:c.-19+17432A>C	XP_011518931.1:n.-19+17432A>C
XM_011520630.1:c.-19+17432A>C	XP_011518932.1:n.-19+17432A>C
NM_000834.4:c.-19+17432A>C	NP_000825.2:n.-19+17432A>C
XM_011520628.2:c.-19+17432A>C	XP_011518930.1:n.-19+17432A>C
XM_011520629.2:c.-19+17432A>C	XP_011518931.1:n.-19+17432A>C
XM_017019219.2:c.-19+17432A>C	XP_016874708.1:n.-19+17432A>C
NM_000834.5:c.-19+17432A>C MANE Select	NP_000825.2:n.-19+17432A>C