Canonical Allele Identifier: CA1768218948
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400368A= , CM000670.2:g.18400368A= GRCh38
NC_000008.10:g.18257878A= , CM000670.1:g.18257878A= GRCh37
NC_000008.9:g.18302158A= NCBI36
NG_012246.1:g.14124A=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.365A= MANE Select ENSP00000286479.3:p.Asp122=
ENST00000286479.3:c.365A= ENSP00000286479.3:p.Asp122=
ENST00000520116.1:c.-26A= ENSP00000428416.1:n.-26A=
NM_000015.2:c.365A= NP_000006.2:p.Asp122=
XM_011544358.1:c.365A= XP_011542660.1:p.Asp122=
XM_017012938.1:c.365A= XP_016868427.1:p.Asp122=
NM_000015.3:c.365A= MANE Select NP_000006.2:p.Asp122=