Canonical Allele Identifier: CA1250108728
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs995868717

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51440630A>C , CM000664.2:g.51440630A>C GRCh38
NC_000002.11:g.51667768A>C , CM000664.1:g.51667768A>C GRCh37
NC_000002.10:g.51521272A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_245003.1:n.694+62457A>C
NR_135237.1:n.694+62457A>C