Canonical Allele Identifier: CA2474156931
Gene: NSUN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46368571C= , CM000663.2:g.46368571C= GRCh38
NC_000001.10:g.46834243C= , CM000663.1:g.46834243C= GRCh37
NC_000001.9:g.46606830C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001387266.1:c.*702C= NP_001374195.1:n.*702C=
NM_001387268.1:c.1006-201C= NP_001374197.1:n.1006-201C=
NM_001387269.1:c.*183C= NP_001374198.1:n.*183C=
NM_001387270.1:c.878+7743C= NP_001374199.1:n.878+7743C=