Canonical Allele Identifier: CA1768219053
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400589C= , CM000670.2:g.18400589C= GRCh38
NC_000008.10:g.18258099C= , CM000670.1:g.18258099C= GRCh37
NC_000008.9:g.18302379C= NCBI36
NG_012246.1:g.14345C=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.586C= MANE Select ENSP00000286479.3:p.Pro196=
ENST00000286479.3:c.586C= ENSP00000286479.3:p.Pro196=
ENST00000520116.1:c.196C= ENSP00000428416.1:p.Pro66=
NM_000015.2:c.586C= NP_000006.2:p.Pro196=
XM_011544358.1:c.586C= XP_011542660.1:p.Pro196=
XM_017012938.1:c.586C= XP_016868427.1:p.Pro196=
NM_000015.3:c.586C= MANE Select NP_000006.2:p.Pro196=