Canonical Allele Identifier: CA459881306

Gene: NAT2

Linked Data

• MyVariant Identifiers: chr8:g.18258155A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18400645A>G , CM000670.2:g.18400645A>G	GRCh38
NC_000008.10:g.18258155A>G , CM000670.1:g.18258155A>G	GRCh37
NC_000008.9:g.18302435A>G	NCBI36
NG_012246.1:g.14401A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.642A>G MANE Select	ENSP00000286479.3:p.Thr214=
ENST00000286479.3:c.642A>G	ENSP00000286479.3:p.Thr214=
ENST00000520116.1:c.252A>G	ENSP00000428416.1:p.Thr84=
NM_000015.2:c.642A>G	NP_000006.2:p.Thr214=
XM_011544358.1:c.642A>G	XP_011542660.1:p.Thr214=
XM_017012938.1:c.642A>G	XP_016868427.1:p.Thr214=
NM_000015.3:c.642A>G MANE Select	NP_000006.2:p.Thr214=