Canonical Allele Identifier: CA736271901

Gene: NSUN4

Linked Data

• dbSNP Id: rs1023070065
• gnomAD v3: 1-46368555-G-T
• gnomAD v4: 1-46368555-G-T
• MyVariant Identifiers: chr1:g.46834227G>T (hg19) ; chr1:g.46368555G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46368555G>T , CM000663.2:g.46368555G>T	GRCh38
NC_000001.10:g.46834227G>T , CM000663.1:g.46834227G>T	GRCh37
NC_000001.9:g.46606814G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NM_001387266.1:c.*686G>T	NP_001374195.1:n.*686G>T
NM_001387268.1:c.1006-217G>T	NP_001374197.1:n.1006-217G>T
NM_001387269.1:c.*167G>T	NP_001374198.1:n.*167G>T
NM_001387270.1:c.878+7727G>T	NP_001374199.1:n.878+7727G>T