Canonical Allele Identifier: CA1768219046
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400573C= , CM000670.2:g.18400573C= GRCh38
NC_000008.10:g.18258083C= , CM000670.1:g.18258083C= GRCh37
NC_000008.9:g.18302363C= NCBI36
NG_012246.1:g.14329C=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.570C= MANE Select ENSP00000286479.3:p.Tyr190=
ENST00000286479.3:c.570C= ENSP00000286479.3:p.Tyr190=
ENST00000520116.1:c.180C= ENSP00000428416.1:p.Tyr60=
NM_000015.2:c.570C= NP_000006.2:p.Tyr190=
XM_011544358.1:c.570C= XP_011542660.1:p.Tyr190=
XM_017012938.1:c.570C= XP_016868427.1:p.Tyr190=
NM_000015.3:c.570C= MANE Select NP_000006.2:p.Tyr190=