Canonical Allele Identifier: CA1768219071
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400616A= , CM000670.2:g.18400616A= GRCh38
NC_000008.10:g.18258126A= , CM000670.1:g.18258126A= GRCh37
NC_000008.9:g.18302406A= NCBI36
NG_012246.1:g.14372A=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.613A= MANE Select ENSP00000286479.3:p.Met205=
ENST00000286479.3:c.613A= ENSP00000286479.3:p.Met205=
ENST00000520116.1:c.223A= ENSP00000428416.1:p.Met75=
NM_000015.2:c.613A= NP_000006.2:p.Met205=
XM_011544358.1:c.613A= XP_011542660.1:p.Met205=
XM_017012938.1:c.613A= XP_016868427.1:p.Met205=
NM_000015.3:c.613A= MANE Select NP_000006.2:p.Met205=