Canonical Allele Identifier: CA2474156925
Gene: NSUN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46368558T= , CM000663.2:g.46368558T= GRCh38
NC_000001.10:g.46834230T= , CM000663.1:g.46834230T= GRCh37
NC_000001.9:g.46606817T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001387266.1:c.*689T= NP_001374195.1:n.*689T=
NM_001387268.1:c.1006-214T= NP_001374197.1:n.1006-214T=
NM_001387269.1:c.*170T= NP_001374198.1:n.*170T=
NM_001387270.1:c.878+7730T= NP_001374199.1:n.878+7730T=