Canonical Allele Identifier: CA9030403
Gene: GRIN3B HGNC NCBI

Linked Data

dbSNP Id: rs748647527
ExAC: 19:1004897 G / GTTT
gnomAD v2: 19-1004897-G-GTTT
gnomAD v4: 19-1004898-G-GTTT
MyVariant Identifiers: chr19:g.1004897_1004898insTTT (hg19) chr19:g.1004898_1004899insTTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1004898_1004899insTTT , CM000681.2:g.1004898_1004899insTTT GRCh38
NC_000019.9:g.1004897_1004898insTTT , CM000681.1:g.1004897_1004898insTTT GRCh37
NC_000019.8:g.955897_955898insTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234389.3:c.1397_1398insTTT MANE Select ENSP00000234389.3:p.Gly466_Ser467insPhe
ENST00000588335.1:n.147_148insTTT
NM_138690.1:c.1397_1398insTTT NP_619635.1:p.Gly466_Ser467insPhe
NM_138690.2:c.1397_1398insTTT NP_619635.1:p.Gly466_Ser467insPhe
XM_017026243.2:c.-182_-181insTTT XP_016881732.1:n.-182_-181insTTT
NM_138690.3:c.1397_1398insTTT MANE Select NP_619635.1:p.Gly466_Ser467insPhe
Search 100 bp 5'
Search 100 bp 3'