Canonical Allele Identifier: CA1768218937
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400349G= , CM000670.2:g.18400349G= GRCh38
NC_000008.10:g.18257859G= , CM000670.1:g.18257859G= GRCh37
NC_000008.9:g.18302139G= NCBI36
NG_012246.1:g.14105G=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.346G= MANE Select ENSP00000286479.3:p.Gly116=
ENST00000286479.3:c.346G= ENSP00000286479.3:p.Gly116=
ENST00000520116.1:c.-45G= ENSP00000428416.1:n.-45G=
NM_000015.2:c.346G= NP_000006.2:p.Gly116=
XM_011544358.1:c.346G= XP_011542660.1:p.Gly116=
XM_017012938.1:c.346G= XP_016868427.1:p.Gly116=
NM_000015.3:c.346G= MANE Select NP_000006.2:p.Gly116=