Canonical Allele Identifier: CA50370820

Gene: NAT8

Linked Data

• dbSNP Id: rs938586991
• MyVariant Identifiers: chr2:g.73868069A>T (hg19) ; chr2:g.73640942A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73640942A>T , CM000664.2:g.73640942A>T	GRCh38
NC_000002.11:g.73868069A>T , CM000664.1:g.73868069A>T	GRCh37
NC_000002.10:g.73721577A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272425.4:c.*3T>A MANE Select	ENSP00000272425.3:n.*3T>A
ENST00000272425.3:c.*3T>A	ENSP00000272425.3:n.*3T>A
NM_003960.3:c.*3T>A	NP_003951.3:n.*3T>A
NM_003960.4:c.*3T>A MANE Select	NP_003951.3:n.*3T>A