Canonical Allele Identifier: CA1768218943
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400357T= , CM000670.2:g.18400357T= GRCh38
NC_000008.10:g.18257867T= , CM000670.1:g.18257867T= GRCh37
NC_000008.9:g.18302147T= NCBI36
NG_012246.1:g.14113T=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.354T= MANE Select ENSP00000286479.3:p.Asn118=
ENST00000286479.3:c.354T= ENSP00000286479.3:p.Asn118=
ENST00000520116.1:c.-37T= ENSP00000428416.1:n.-37T=
NM_000015.2:c.354T= NP_000006.2:p.Asn118=
XM_011544358.1:c.354T= XP_011542660.1:p.Asn118=
XM_017012938.1:c.354T= XP_016868427.1:p.Asn118=
NM_000015.3:c.354T= MANE Select NP_000006.2:p.Asn118=