Canonical Allele Identifier: CA1768218920
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400311C= , CM000670.2:g.18400311C= GRCh38
NC_000008.10:g.18257821C= , CM000670.1:g.18257821C= GRCh37
NC_000008.9:g.18302101C= NCBI36
NG_012246.1:g.14067C=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.308C= MANE Select ENSP00000286479.3:p.Thr103=
ENST00000286479.3:c.308C= ENSP00000286479.3:p.Thr103=
ENST00000520116.1:c.-57-26C= ENSP00000428416.1:n.-57-26C=
NM_000015.2:c.308C= NP_000006.2:p.Thr103=
XM_011544358.1:c.308C= XP_011542660.1:p.Thr103=
XM_017012938.1:c.308C= XP_016868427.1:p.Thr103=
NM_000015.3:c.308C= MANE Select NP_000006.2:p.Thr103=