Canonical Allele Identifier: CA532694306
Gene: NRXN1-DT HGNC NCBI

Linked Data

dbSNP Id: rs1198654554
gnomAD v2: 2-52072152-A-G
gnomAD v3: 2-51845014-A-G
gnomAD v4: 2-51845014-A-G
MyVariant Identifiers: chr2:g.52072152A>G (hg19) chr2:g.51845014A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.51845014A>G , CM000664.2:g.51845014A>G GRCh38
NC_000002.11:g.52072152A>G , CM000664.1:g.52072152A>G GRCh37
NC_000002.10:g.51925656A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245003.1:n.840-16435A>G
NR_135237.1:n.840-16435A>G
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