Canonical Allele Identifier: CA2317457795

Gene: GRIN3B

Linked Data

• dbSNP Id: rs2038727198
• gnomAD v4: 19-1004898-GCTCAGCGCCCCGTGCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1004901_1004916del , CM000681.2:g.1004901_1004916del	GRCh38
NC_000019.9:g.1004900_1004915del , CM000681.1:g.1004900_1004915del	GRCh37
NC_000019.8:g.955900_955915del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234389.3:c.1400_1415del MANE Select	ENSP00000234389.3:p.Ser467CysfsTer?
ENST00000588335.1:n.150_165del
NM_138690.1:c.1400_1415del	NP_619635.1:p.Ser467CysfsTer?
NM_138690.2:c.1400_1415del	NP_619635.1:p.Ser467CysfsTer?
XM_017026243.2:c.-179_-164del	XP_016881732.1:n.-179_-164del
NM_138690.3:c.1400_1415del MANE Select	NP_619635.1:p.Ser467CysfsTer?