Canonical Allele Identifier: CA10724068
Gene: NSUN4 HGNC NCBI

Linked Data

dbSNP Id: rs59082884
gnomAD v2: 1-46834249-G-A
gnomAD v3: 1-46368577-G-A
gnomAD v4: 1-46368577-G-A
MyVariant Identifiers: chr1:g.46834249G>A (hg19) chr1:g.46368577G>A (hg38)
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Genomic Alleles

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

Transcript Alleles

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