Canonical Allele Identifier: CA504884395

Gene: GRIN3B

Linked Data

• gnomAD v4: 19-1004905-G-T
• MyVariant Identifiers: chr19:g.1004904G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1004905G>T , CM000681.2:g.1004905G>T	GRCh38
NC_000019.9:g.1004904G>T , CM000681.1:g.1004904G>T	GRCh37
NC_000019.8:g.955904G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234389.3:c.1404G>T MANE Select	ENSP00000234389.3:p.Ala468=
ENST00000588335.1:n.154G>T
NM_138690.1:c.1404G>T	NP_619635.1:p.Ala468=
NM_138690.2:c.1404G>T	NP_619635.1:p.Ala468=
XM_017026243.2:c.-175G>T	XP_016881732.1:n.-175G>T
NM_138690.3:c.1404G>T MANE Select	NP_619635.1:p.Ala468=