Canonical Allele Identifier: CA2575085730

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13615014-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615014A>G , CM000674.2:g.13615014A>G	GRCh38
NC_000012.11:g.13767948A>G , CM000674.1:g.13767948A>G	GRCh37
NC_000012.10:g.13659215A>G	NCBI36
NG_031854.1:g.370075T>C
NG_031854.2:g.371999T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1654+100T>C MANE Select	ENSP00000477455.1:n.1654+100T>C
ENST00000609686.3:c.1654+100T>C	ENSP00000477455.1:n.1654+100T>C
NM_000834.3:c.1654+100T>C	NP_000825.2:n.1654+100T>C
XM_011520628.1:c.1654+100T>C	XP_011518930.1:n.1654+100T>C
XM_011520629.1:c.1654+100T>C	XP_011518931.1:n.1654+100T>C
XM_011520630.1:c.1654+100T>C	XP_011518932.1:n.1654+100T>C
XR_931372.1:n.179-84A>G
XR_931373.1:n.319-84A>G
XR_931374.1:n.118-84A>G
NM_000834.4:c.1654+100T>C	NP_000825.2:n.1654+100T>C
XM_011520628.2:c.1654+100T>C	XP_011518930.1:n.1654+100T>C
XM_011520629.2:c.1654+100T>C	XP_011518931.1:n.1654+100T>C
XM_017019219.2:c.1654+100T>C	XP_016874708.1:n.1654+100T>C
XR_001749013.1:n.600-84A>G
XR_931372.2:n.316-84A>G
XR_931373.2:n.458-84A>G
NM_000834.5:c.1654+100T>C MANE Select	NP_000825.2:n.1654+100T>C