Canonical Allele Identifier: CA1715706
Gene: NAT8 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs13538

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73641201A>G , CM000664.2:g.73641201A>G GRCh38
NC_000002.11:g.73868328A>G , CM000664.1:g.73868328A>G GRCh37
NC_000002.10:g.73721836A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_003960.3:c.428T>C VV NP_003951.3:p.Phe143Ser
ENST00000272425.3:c.428T>C ENSP00000272425.3:p.Phe143Ser