Canonical Allele Identifier: CA384051760

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13768091C>G (hg19) ; chr12:g.13615157C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615157C>G , CM000674.2:g.13615157C>G	GRCh38
NC_000012.11:g.13768091C>G , CM000674.1:g.13768091C>G	GRCh37
NC_000012.10:g.13659358C>G	NCBI36
NG_031854.1:g.369932G>C
NG_031854.2:g.371856G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1611G>C MANE Select	ENSP00000477455.1:p.Met537Ile
ENST00000609686.3:c.1611G>C	ENSP00000477455.1:p.Met537Ile
NM_000834.3:c.1611G>C	NP_000825.2:p.Met537Ile
XM_011520628.1:c.1611G>C	XP_011518930.1:p.Met537Ile
XM_011520629.1:c.1611G>C	XP_011518931.1:p.Met537Ile
XM_011520630.1:c.1611G>C	XP_011518932.1:p.Met537Ile
XR_931372.1:n.238C>G
XR_931373.1:n.378C>G
XR_931374.1:n.177C>G
NM_000834.4:c.1611G>C	NP_000825.2:p.Met537Ile
XM_011520628.2:c.1611G>C	XP_011518930.1:p.Met537Ile
XM_011520629.2:c.1611G>C	XP_011518931.1:p.Met537Ile
XM_017019219.2:c.1611G>C	XP_016874708.1:p.Met537Ile
XR_001749013.1:n.659C>G
XR_931372.2:n.375C>G
XR_931373.2:n.517C>G
NM_000834.5:c.1611G>C MANE Select	NP_000825.2:p.Met537Ile