Canonical Allele Identifier: CA370635350
Gene: NAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400190A>T , CM000670.2:g.18400190A>T GRCh38
NC_000008.10:g.18257700A>T , CM000670.1:g.18257700A>T GRCh37
NC_000008.9:g.18301980A>T NCBI36
NG_012246.1:g.13946A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.187A>T MANE Select ENSP00000286479.3:p.Asn63Tyr
ENST00000286479.3:c.187A>T ENSP00000286479.3:p.Asn63Tyr
ENST00000520116.1:c.-57-147A>T ENSP00000428416.1:n.-57-147A>T
NM_000015.2:c.187A>T NP_000006.2:p.Asn63Tyr
XM_011544358.1:c.187A>T XP_011542660.1:p.Asn63Tyr
XM_017012938.1:c.187A>T XP_016868427.1:p.Asn63Tyr
NM_000015.3:c.187A>T MANE Select NP_000006.2:p.Asn63Tyr