Canonical Allele Identifier: CA1030634439
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1671955882
gnomAD v3: 2-51844967-C-A
gnomAD v4: 2-51844967-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51844967C>A , CM000664.2:g.51844967C>A GRCh38
NC_000002.11:g.52072105C>A , CM000664.1:g.52072105C>A GRCh37
NC_000002.10:g.51925609C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16482C>A
NR_135237.1:n.840-16482C>A