Canonical Allele Identifier: CA1140337813
Gene: NSUN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46368540T= , CM000663.2:g.46368540T= GRCh38
NC_000001.10:g.46834212T= , CM000663.1:g.46834212T= GRCh37
NC_000001.9:g.46606799T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001387266.1:c.*671T= NP_001374195.1:n.*671T=
NM_001387268.1:c.1006-232T= NP_001374197.1:n.1006-232T=
NM_001387269.1:c.*152T= NP_001374198.1:n.*152T=
NM_001387270.1:c.878+7712T= NP_001374199.1:n.878+7712T=