Canonical Allele Identifier: CA857768810
Gene: GRIN3A HGNC NCBI

Linked Data

dbSNP Id: rs1247155715
gnomAD v3: 9-101585888-GCAATGGGCTATGAGGCCTCA-G
gnomAD v4: 9-101585888-GCAATGGGCTATGAGGCCTCA-G
MyVariant Identifiers: chr9:g.104348171_104348190del (hg19) chr9:g.101585889_101585908del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.101585892_101585911del , CM000671.2:g.101585892_101585911del GRCh38
NC_000009.11:g.104348174_104348193del , CM000671.1:g.104348174_104348193del GRCh37
NC_000009.10:g.103387995_103388014del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361820.6:c.2767-6548_2767-6529del MANE Select ENSP00000355155.3:n.2767-6548_2767-6529de...
ENST00000361820.3:c.2767-6548_2767-6529del ENSP00000355155.3:n.2767-6548_2767-6529de...
NM_133445.2:c.2767-6548_2767-6529del NP_597702.2:n.2767-6548_2767-6529del
NM_133445.3:c.2767-6548_2767-6529del MANE Select NP_597702.2:n.2767-6548_2767-6529del
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