Canonical Allele Identifier: CA9030401
Gene: GRIN3B HGNC NCBI
gnomAD v2:
19:1004896 G / GCGTT
gnomAD v3:
19:1004897 G / GCGTT
gnomAD v4:
chr19-1004897-G-GCGTT
Joint Max Group AF 0.30513334 (NFE)
Genomes Max Group AF 0.30113962 (NFE)
Exomes Max Group AF 0.30519055 (NFE)
dbSNP:
10666583
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1004897_1004898insCGTT , CM000681.2:g.1004897_1004898insCGTT GRCh38
NC_000019.9:g.1004896_1004897insCGTT , CM000681.1:g.1004896_1004897insCGTT GRCh37
NC_000019.8:g.955896_955897insCGTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234389.3:c.1396_1397insCGTT MANE Select ENSP00000234389.3:p.Gly466AlafsTer18
ENST00000588335.1:n.146_147insCGTT
NM_138690.1:c.1396_1397insCGTT NP_619635.1:p.Gly466AlafsTer18
NM_138690.2:c.1396_1397insCGTT NP_619635.1:p.Gly466AlafsTer18
XM_017026243.2:c.-183_-182insCGTT XP_016881732.1:n.-183_-182insCGTT
NM_138690.3:c.1396_1397insCGTT MANE Select NP_619635.1:p.Gly466AlafsTer18
Search 100 bp 5'
Search 100 bp 3'