Canonical Allele Identifier: CA1030586971
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1667702764
gnomAD v3: 2-51440645-A-C
gnomAD v4: 2-51440645-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51440645A>C , CM000664.2:g.51440645A>C GRCh38
NC_000002.11:g.51667783A>C , CM000664.1:g.51667783A>C GRCh37
NC_000002.10:g.51521287A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.694+62472A>C
NR_135237.1:n.694+62472A>C