Canonical Allele Identifier: CA1768219119
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400726T= , CM000670.2:g.18400726T= GRCh38
NC_000008.10:g.18258236T= , CM000670.1:g.18258236T= GRCh37
NC_000008.9:g.18302516T= NCBI36
NG_012246.1:g.14482T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.723T= MANE Select ENSP00000286479.3:p.Tyr241=
ENST00000286479.3:c.723T= ENSP00000286479.3:p.Tyr241=
ENST00000520116.1:c.333T= ENSP00000428416.1:p.Tyr111=
NM_000015.2:c.723T= NP_000006.2:p.Tyr241=
XM_011544358.1:c.723T= XP_011542660.1:p.Tyr241=
XM_017012938.1:c.723T= XP_016868427.1:p.Tyr241=
NM_000015.3:c.723T= MANE Select NP_000006.2:p.Tyr241=