Canonical Allele Identifier: CA736271907

Gene: NSUN4

Linked Data

• dbSNP Id: rs1478668938
• MyVariant Identifiers: chr1:g.46834232G>A (hg19) ; chr1:g.46368560G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46368560G>A , CM000663.2:g.46368560G>A	GRCh38
NC_000001.10:g.46834232G>A , CM000663.1:g.46834232G>A	GRCh37
NC_000001.9:g.46606819G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NM_001387266.1:c.*691G>A	NP_001374195.1:n.*691G>A
NM_001387268.1:c.1006-212G>A	NP_001374197.1:n.1006-212G>A
NM_001387269.1:c.*172G>A	NP_001374198.1:n.*172G>A
NM_001387270.1:c.878+7732G>A	NP_001374199.1:n.878+7732G>A