Canonical Allele Identifier: CA233010992

Gene: GRIN2B

Linked Data

• dbSNP Id: rs546200098
• gnomAD v2: 12-13767820-T-G
• gnomAD v3: 12-13614886-T-G
• gnomAD v4: 12-13614886-T-G
• MyVariant Identifiers: chr12:g.13767820T>G (hg19) ; chr12:g.13614886T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13614886T>G , CM000674.2:g.13614886T>G	GRCh38
NC_000012.11:g.13767820T>G , CM000674.1:g.13767820T>G	GRCh37
NC_000012.10:g.13659087T>G	NCBI36
NG_031854.1:g.370203A>C
NG_031854.2:g.372127A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1654+228A>C MANE Select	ENSP00000477455.1:n.1654+228A>C
ENST00000609686.3:c.1654+228A>C	ENSP00000477455.1:n.1654+228A>C
NM_000834.3:c.1654+228A>C	NP_000825.2:n.1654+228A>C
XM_011520628.1:c.1654+228A>C	XP_011518930.1:n.1654+228A>C
XM_011520629.1:c.1654+228A>C	XP_011518931.1:n.1654+228A>C
XM_011520630.1:c.1654+228A>C	XP_011518932.1:n.1654+228A>C
XR_931372.1:n.179-212T>G
XR_931373.1:n.319-212T>G
XR_931374.1:n.118-212T>G
NM_000834.4:c.1654+228A>C	NP_000825.2:n.1654+228A>C
XM_011520628.2:c.1654+228A>C	XP_011518930.1:n.1654+228A>C
XM_011520629.2:c.1654+228A>C	XP_011518931.1:n.1654+228A>C
XM_017019219.2:c.1654+228A>C	XP_016874708.1:n.1654+228A>C
XR_001749013.1:n.600-212T>G
XR_931372.2:n.316-212T>G
XR_931373.2:n.458-212T>G
NM_000834.5:c.1654+228A>C MANE Select	NP_000825.2:n.1654+228A>C