Canonical Allele Identifier: CA370635577
Gene: NAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400299A>T , CM000670.2:g.18400299A>T GRCh38
NC_000008.10:g.18257809A>T , CM000670.1:g.18257809A>T GRCh37
NC_000008.9:g.18302089A>T NCBI36
NG_012246.1:g.14055A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.296A>T MANE Select ENSP00000286479.3:p.Asn99Ile
ENST00000286479.3:c.296A>T ENSP00000286479.3:p.Asn99Ile
ENST00000520116.1:c.-57-38A>T ENSP00000428416.1:n.-57-38A>T
NM_000015.2:c.296A>T NP_000006.2:p.Asn99Ile
XM_011544358.1:c.296A>T XP_011542660.1:p.Asn99Ile
XM_017012938.1:c.296A>T XP_016868427.1:p.Asn99Ile
NM_000015.3:c.296A>T MANE Select NP_000006.2:p.Asn99Ile