Canonical Allele Identifier: CA459699823

Gene: NAT2

Linked Data

• MyVariant Identifiers: chr8:g.18258311G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18400801G>C , CM000670.2:g.18400801G>C	GRCh38
NC_000008.10:g.18258311G>C , CM000670.1:g.18258311G>C	GRCh37
NC_000008.9:g.18302591G>C	NCBI36
NG_012246.1:g.14557G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.798G>C MANE Select	ENSP00000286479.3:p.Val266=
ENST00000286479.3:c.798G>C	ENSP00000286479.3:p.Val266=
ENST00000520116.1:c.408G>C	ENSP00000428416.1:p.Val136=
NM_000015.2:c.798G>C	NP_000006.2:p.Val266=
XM_011544358.1:c.798G>C	XP_011542660.1:p.Val266=
XM_017012938.1:c.798G>C	XP_016868427.1:p.Val266=
NM_000015.3:c.798G>C MANE Select	NP_000006.2:p.Val266=