Canonical Allele Identifier: CA233159109

Gene: GRIN2B

Linked Data

• dbSNP Id: rs945692607
• gnomAD v3: 12-13962510-A-G
• gnomAD v4: 12-13962510-A-G
• MyVariant Identifiers: chr12:g.14115444A>G (hg19) ; chr12:g.13962510A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13962510A>G , CM000674.2:g.13962510A>G	GRCh38
NC_000012.11:g.14115444A>G , CM000674.1:g.14115444A>G	GRCh37
NC_000012.10:g.14006711A>G	NCBI36
NG_031854.1:g.22579T>C
NG_031854.2:g.24503T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.-19+17418T>C MANE Select	ENSP00000477455.1:n.-19+17418T>C
ENST00000630791.2:c.-19+17418T>C	ENSP00000486677.2:n.-19+17418T>C
ENST00000609686.3:c.-19+17418T>C	ENSP00000477455.1:n.-19+17418T>C
ENST00000627535.2:c.-19+17418T>C	ENSP00000486411.1:n.-19+17418T>C
ENST00000630791.1:c.-19+17418T>C	ENSP00000486677.1:n.-19+17418T>C
NM_000834.3:c.-19+17418T>C	NP_000825.2:n.-19+17418T>C
XM_011520628.1:c.-19+17418T>C	XP_011518930.1:n.-19+17418T>C
XM_011520629.1:c.-19+17418T>C	XP_011518931.1:n.-19+17418T>C
XM_011520630.1:c.-19+17418T>C	XP_011518932.1:n.-19+17418T>C
NM_000834.4:c.-19+17418T>C	NP_000825.2:n.-19+17418T>C
XM_011520628.2:c.-19+17418T>C	XP_011518930.1:n.-19+17418T>C
XM_011520629.2:c.-19+17418T>C	XP_011518931.1:n.-19+17418T>C
XM_017019219.2:c.-19+17418T>C	XP_016874708.1:n.-19+17418T>C
NM_000834.5:c.-19+17418T>C MANE Select	NP_000825.2:n.-19+17418T>C