Canonical Allele Identifier: CA1768218891
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400252T= , CM000670.2:g.18400252T= GRCh38
NC_000008.10:g.18257762T= , CM000670.1:g.18257762T= GRCh37
NC_000008.9:g.18302042T= NCBI36
NG_012246.1:g.14008T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.249T= MANE Select ENSP00000286479.3:p.Gly83=
ENST00000286479.3:c.249T= ENSP00000286479.3:p.Gly83=
ENST00000520116.1:c.-57-85T= ENSP00000428416.1:n.-57-85T=
NM_000015.2:c.249T= NP_000006.2:p.Gly83=
XM_011544358.1:c.249T= XP_011542660.1:p.Gly83=
XM_017012938.1:c.249T= XP_016868427.1:p.Gly83=
NM_000015.3:c.249T= MANE Select NP_000006.2:p.Gly83=