Canonical Allele Identifier: CA769932158
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1308668973
MyVariant Identifiers: chr2:g.52072607C>G (hg19) chr2:g.51845469C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845469C>G , CM000664.2:g.51845469C>G GRCh38
NC_000002.11:g.52072607C>G , CM000664.1:g.52072607C>G GRCh37
NC_000002.10:g.51926111C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-15980C>G
NR_135237.1:n.840-15980C>G
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