Canonical Allele Identifier: CA1140809530
Gene: NSUN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46368579G= , CM000663.2:g.46368579G= GRCh38
NC_000001.10:g.46834251G= , CM000663.1:g.46834251G= GRCh37
NC_000001.9:g.46606838G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001387266.1:c.*710G= NP_001374195.1:n.*710G=
NM_001387268.1:c.1006-193G= NP_001374197.1:n.1006-193G=
NM_001387269.1:c.*191G= NP_001374198.1:n.*191G=
NM_001387270.1:c.878+7751G= NP_001374199.1:n.878+7751G=