Canonical Allele Identifier: CA1768218942
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400356A= , CM000670.2:g.18400356A= GRCh38
NC_000008.10:g.18257866A= , CM000670.1:g.18257866A= GRCh37
NC_000008.9:g.18302146A= NCBI36
NG_012246.1:g.14112A=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.353A= MANE Select ENSP00000286479.3:p.Asn118=
ENST00000286479.3:c.353A= ENSP00000286479.3:p.Asn118=
ENST00000520116.1:c.-38A= ENSP00000428416.1:n.-38A=
NM_000015.2:c.353A= NP_000006.2:p.Asn118=
XM_011544358.1:c.353A= XP_011542660.1:p.Asn118=
XM_017012938.1:c.353A= XP_016868427.1:p.Asn118=
NM_000015.3:c.353A= MANE Select NP_000006.2:p.Asn118=