Canonical Allele Identifier: CA1001343166
Gene: NSUN4 HGNC NCBI

Linked Data

dbSNP Id: rs1664188938
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46368583C>A , CM000663.2:g.46368583C>A GRCh38
NC_000001.10:g.46834255C>A , CM000663.1:g.46834255C>A GRCh37
NC_000001.9:g.46606842C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001387266.1:c.*714C>A NP_001374195.1:n.*714C>A
NM_001387268.1:c.1006-189C>A NP_001374197.1:n.1006-189C>A
NM_001387269.1:c.*195C>A NP_001374198.1:n.*195C>A
NM_001387270.1:c.878+7755C>A NP_001374199.1:n.878+7755C>A
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