Canonical Allele Identifier: CA1768218922
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400312T= , CM000670.2:g.18400312T= GRCh38
NC_000008.10:g.18257822T= , CM000670.1:g.18257822T= GRCh37
NC_000008.9:g.18302102T= NCBI36
NG_012246.1:g.14068T=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.309T= MANE Select ENSP00000286479.3:p.Thr103=
ENST00000286479.3:c.309T= ENSP00000286479.3:p.Thr103=
ENST00000520116.1:c.-57-25T= ENSP00000428416.1:n.-57-25T=
NM_000015.2:c.309T= NP_000006.2:p.Thr103=
XM_011544358.1:c.309T= XP_011542660.1:p.Thr103=
XM_017012938.1:c.309T= XP_016868427.1:p.Thr103=
NM_000015.3:c.309T= MANE Select NP_000006.2:p.Thr103=