Canonical Allele Identifier: CA685703440

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1380093566
• gnomAD v4: 12-13981830-G-A
• MyVariant Identifiers: chr12:g.14134764G>A (hg19) ; chr12:g.13981830G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13981830G>A , CM000674.2:g.13981830G>A	GRCh38
NC_000012.11:g.14134764G>A , CM000674.1:g.14134764G>A	GRCh37
NC_000012.10:g.14026031G>A	NCBI36
NG_031854.1:g.3259C>T
NG_031854.2:g.5183C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000630791.2:c.-683+86C>T	ENSP00000486677.2:n.-683+86C>T
ENST00000627535.2:c.-448+86C>T	ENSP00000486411.1:n.-448+86C>T
ENST00000630791.1:c.-683+86C>T	ENSP00000486677.1:n.-683+86C>T
XM_011520629.1:c.-683+86C>T	XP_011518931.1:n.-683+86C>T
XM_011520628.2:c.-936C>T	XP_011518930.1:n.-936C>T
XM_011520629.2:c.-683+86C>T	XP_011518931.1:n.-683+86C>T