Canonical Allele Identifier: CA1768219048
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400581C= , CM000670.2:g.18400581C= GRCh38
NC_000008.10:g.18258091C= , CM000670.1:g.18258091C= GRCh37
NC_000008.9:g.18302371C= NCBI36
NG_012246.1:g.14337C=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.578C= MANE Select ENSP00000286479.3:p.Thr193=
ENST00000286479.3:c.578C= ENSP00000286479.3:p.Thr193=
ENST00000520116.1:c.188C= ENSP00000428416.1:p.Thr63=
NM_000015.2:c.578C= NP_000006.2:p.Thr193=
XM_011544358.1:c.578C= XP_011542660.1:p.Thr193=
XM_017012938.1:c.578C= XP_016868427.1:p.Thr193=
NM_000015.3:c.578C= MANE Select NP_000006.2:p.Thr193=