Canonical Allele Identifier: CA504884398

Gene: GRIN3B

Linked Data

• MyVariant Identifiers: chr19:g.1004907C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1004908C>T , CM000681.2:g.1004908C>T	GRCh38
NC_000019.9:g.1004907C>T , CM000681.1:g.1004907C>T	GRCh37
NC_000019.8:g.955907C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000234389.3:c.1407C>T MANE Select	ENSP00000234389.3:p.Pro469=
ENST00000588335.1:n.157C>T
NM_138690.1:c.1407C>T	NP_619635.1:p.Pro469=
NM_138690.2:c.1407C>T	NP_619635.1:p.Pro469=
XM_017026243.2:c.-172C>T	XP_016881732.1:n.-172C>T
NM_138690.3:c.1407C>T MANE Select	NP_619635.1:p.Pro469=