Canonical Allele Identifier: CA1140682690
Gene: NSUN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46368577G= , CM000663.2:g.46368577G= GRCh38
NC_000001.10:g.46834249G= , CM000663.1:g.46834249G= GRCh37
NC_000001.9:g.46606836G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001387266.1:c.*708G= NP_001374195.1:n.*708G=
NM_001387268.1:c.1006-195G= NP_001374197.1:n.1006-195G=
NM_001387269.1:c.*189G= NP_001374198.1:n.*189G=
NM_001387270.1:c.878+7749G= NP_001374199.1:n.878+7749G=