Canonical Allele Identifier: CA347285979

Gene: NAT8

Linked Data

• dbSNP Id: rs1436162166
• MyVariant Identifiers: chr2:g.73868078A>C (hg19) ; chr2:g.73640951A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73640951A>C , CM000664.2:g.73640951A>C	GRCh38
NC_000002.11:g.73868078A>C , CM000664.1:g.73868078A>C	GRCh37
NC_000002.10:g.73721586A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272425.4:c.678T>G MANE Select	ENSP00000272425.3:p.Ser226Arg
ENST00000272425.3:c.678T>G	ENSP00000272425.3:p.Ser226Arg
NM_003960.3:c.678T>G	NP_003951.3:p.Ser226Arg
NM_003960.4:c.678T>G MANE Select	NP_003951.3:p.Ser226Arg