Canonical Allele Identifier: CA769945991
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs11889995
MyVariant Identifiers: chr2:g.52163410C>A (hg19) chr2:g.51936272C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51936272C>A , CM000664.2:g.51936272C>A GRCh38
NC_000002.11:g.52163410C>A , CM000664.1:g.52163410C>A GRCh37
NC_000002.10:g.52016914C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.879+74784C>A
NR_135237.1:n.879+74784C>A
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