Canonical Allele Identifier: CA1768218953
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400375G= , CM000670.2:g.18400375G= GRCh38
NC_000008.10:g.18257885G= , CM000670.1:g.18257885G= GRCh37
NC_000008.9:g.18302165G= NCBI36
NG_012246.1:g.14131G=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.372G= MANE Select ENSP00000286479.3:p.Gly124=
ENST00000286479.3:c.372G= ENSP00000286479.3:p.Gly124=
ENST00000520116.1:c.-19G= ENSP00000428416.1:n.-19G=
NM_000015.2:c.372G= NP_000006.2:p.Gly124=
XM_011544358.1:c.372G= XP_011542660.1:p.Gly124=
XM_017012938.1:c.372G= XP_016868427.1:p.Gly124=
NM_000015.3:c.372G= MANE Select NP_000006.2:p.Gly124=