Canonical Allele Identifier: CA1768218713
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18399930A= , CM000670.2:g.18399930A= GRCh38
NC_000008.10:g.18257440A= , CM000670.1:g.18257440A= GRCh37
NC_000008.9:g.18301720A= NCBI36
NG_012246.1:g.13686A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.-6-68A= MANE Select ENSP00000286479.3:n.-6-68A=
ENST00000286479.3:c.-6-68A= ENSP00000286479.3:n.-6-68A=
ENST00000520116.1:c.-57-407A= ENSP00000428416.1:n.-57-407A=
NM_000015.2:c.-6-68A= NP_000006.2:n.-6-68A=
XM_011544358.1:c.-6-68A= XP_011542660.1:n.-6-68A=
XM_017012938.1:c.-6-68A= XP_016868427.1:n.-6-68A=
NM_000015.3:c.-6-68A= MANE Select NP_000006.2:n.-6-68A=