Canonical Allele Identifier: CA504884394
Gene: GRIN3B HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.1004904G>C (hg19)

Genomic Alleles

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

Transcript Alleles

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