Canonical Allele Identifier: CA48253038
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs369342889
gnomAD v2: 2-52072199-G-A
gnomAD v3: 2-51845061-G-A
gnomAD v4: 2-51845061-G-A
MyVariant Identifiers: chr2:g.52072199G>A (hg19) chr2:g.51845061G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845061G>A , CM000664.2:g.51845061G>A GRCh38
NC_000002.11:g.52072199G>A , CM000664.1:g.52072199G>A GRCh37
NC_000002.10:g.51925703G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16388G>A
NR_135237.1:n.840-16388G>A
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