Canonical Allele Identifier: CA48253049
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs554051842
gnomAD v2: 2-52072229-AT-A
gnomAD v3: 2-51845091-AT-A
gnomAD v4: 2-51845091-AT-A
MyVariant Identifiers: chr2:g.52072230del (hg19) chr2:g.51845092del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845094del , CM000664.2:g.51845094del GRCh38
NC_000002.11:g.52072232del , CM000664.1:g.52072232del GRCh37
NC_000002.10:g.51925736del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16355del
NR_135237.1:n.840-16355del
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