Canonical Allele Identifier: CA1768218863
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400207T= , CM000670.2:g.18400207T= GRCh38
NC_000008.10:g.18257717T= , CM000670.1:g.18257717T= GRCh37
NC_000008.9:g.18301997T= NCBI36
NG_012246.1:g.13963T=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.204T= MANE Select ENSP00000286479.3:p.Cys68=
ENST00000286479.3:c.204T= ENSP00000286479.3:p.Cys68=
ENST00000520116.1:c.-57-130T= ENSP00000428416.1:n.-57-130T=
NM_000015.2:c.204T= NP_000006.2:p.Cys68=
XM_011544358.1:c.204T= XP_011542660.1:p.Cys68=
XM_017012938.1:c.204T= XP_016868427.1:p.Cys68=
NM_000015.3:c.204T= MANE Select NP_000006.2:p.Cys68=