Canonical Allele Identifier: CA603465607

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1340429504
• gnomAD v2: 12-14115515-C-G
• MyVariant Identifiers: chr12:g.14115515C>G (hg19) ; chr12:g.13962581C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13962581C>G , CM000674.2:g.13962581C>G	GRCh38
NC_000012.11:g.14115515C>G , CM000674.1:g.14115515C>G	GRCh37
NC_000012.10:g.14006782C>G	NCBI36
NG_031854.1:g.22508G>C
NG_031854.2:g.24432G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.-19+17347G>C MANE Select	ENSP00000477455.1:n.-19+17347G>C
ENST00000630791.2:c.-19+17347G>C	ENSP00000486677.2:n.-19+17347G>C
ENST00000609686.3:c.-19+17347G>C	ENSP00000477455.1:n.-19+17347G>C
ENST00000627535.2:c.-19+17347G>C	ENSP00000486411.1:n.-19+17347G>C
ENST00000630791.1:c.-19+17347G>C	ENSP00000486677.1:n.-19+17347G>C
NM_000834.3:c.-19+17347G>C	NP_000825.2:n.-19+17347G>C
XM_011520628.1:c.-19+17347G>C	XP_011518930.1:n.-19+17347G>C
XM_011520629.1:c.-19+17347G>C	XP_011518931.1:n.-19+17347G>C
XM_011520630.1:c.-19+17347G>C	XP_011518932.1:n.-19+17347G>C
NM_000834.4:c.-19+17347G>C	NP_000825.2:n.-19+17347G>C
XM_011520628.2:c.-19+17347G>C	XP_011518930.1:n.-19+17347G>C
XM_011520629.2:c.-19+17347G>C	XP_011518931.1:n.-19+17347G>C
XM_017019219.2:c.-19+17347G>C	XP_016874708.1:n.-19+17347G>C
NM_000834.5:c.-19+17347G>C MANE Select	NP_000825.2:n.-19+17347G>C