Canonical Allele Identifier: CA1768219101
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400691G= , CM000670.2:g.18400691G= GRCh38
NC_000008.10:g.18258201G= , CM000670.1:g.18258201G= GRCh37
NC_000008.9:g.18302481G= NCBI36
NG_012246.1:g.14447G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.688G= MANE Select ENSP00000286479.3:p.Gly230=
ENST00000286479.3:c.688G= ENSP00000286479.3:p.Gly230=
ENST00000520116.1:c.298G= ENSP00000428416.1:p.Gly100=
NM_000015.2:c.688G= NP_000006.2:p.Gly230=
XM_011544358.1:c.688G= XP_011542660.1:p.Gly230=
XM_017012938.1:c.688G= XP_016868427.1:p.Gly230=
NM_000015.3:c.688G= MANE Select NP_000006.2:p.Gly230=