Canonical Allele Identifier: CA459881102
Gene: NAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.18257801T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400291T>A , CM000670.2:g.18400291T>A GRCh38
NC_000008.10:g.18257801T>A , CM000670.1:g.18257801T>A GRCh37
NC_000008.9:g.18302081T>A NCBI36
NG_012246.1:g.14047T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.288T>A MANE Select ENSP00000286479.3:p.Pro96=
ENST00000286479.3:c.288T>A ENSP00000286479.3:p.Pro96=
ENST00000520116.1:c.-57-46T>A ENSP00000428416.1:n.-57-46T>A
NM_000015.2:c.288T>A NP_000006.2:p.Pro96=
XM_011544358.1:c.288T>A XP_011542660.1:p.Pro96=
XM_017012938.1:c.288T>A XP_016868427.1:p.Pro96=
NM_000015.3:c.288T>A MANE Select NP_000006.2:p.Pro96=