Canonical Allele Identifier: CA1768218812
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400112T= , CM000670.2:g.18400112T= GRCh38
NC_000008.10:g.18257622T= , CM000670.1:g.18257622T= GRCh37
NC_000008.9:g.18301902T= NCBI36
NG_012246.1:g.13868T=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.109T= MANE Select ENSP00000286479.3:p.Phe37=
ENST00000286479.3:c.109T= ENSP00000286479.3:p.Phe37=
ENST00000520116.1:c.-57-225T= ENSP00000428416.1:n.-57-225T=
NM_000015.2:c.109T= NP_000006.2:p.Phe37=
XM_011544358.1:c.109T= XP_011542660.1:p.Phe37=
XM_017012938.1:c.109T= XP_016868427.1:p.Phe37=
NM_000015.3:c.109T= MANE Select NP_000006.2:p.Phe37=