Canonical Allele Identifier: CA370636512
Gene: NAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400736A>T , CM000670.2:g.18400736A>T GRCh38
NC_000008.10:g.18258246A>T , CM000670.1:g.18258246A>T GRCh37
NC_000008.9:g.18302526A>T NCBI36
NG_012246.1:g.14492A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.733A>T MANE Select ENSP00000286479.3:p.Asn245Tyr
ENST00000286479.3:c.733A>T ENSP00000286479.3:p.Asn245Tyr
ENST00000520116.1:c.343A>T ENSP00000428416.1:p.Asn115Tyr
NM_000015.2:c.733A>T NP_000006.2:p.Asn245Tyr
XM_011544358.1:c.733A>T XP_011542660.1:p.Asn245Tyr
XM_017012938.1:c.733A>T XP_016868427.1:p.Asn245Tyr
NM_000015.3:c.733A>T MANE Select NP_000006.2:p.Asn245Tyr