Canonical Allele Identifier: CA1030634546
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1671958786
gnomAD v3: 2-51845171-T-G
gnomAD v4: 2-51845171-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845171T>G , CM000664.2:g.51845171T>G GRCh38
NC_000002.11:g.52072309T>G , CM000664.1:g.52072309T>G GRCh37
NC_000002.10:g.51925813T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.840-16278T>G
NR_135237.1:n.840-16278T>G