Canonical Allele Identifier: CA173519937
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs971610227

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400712T>C , CM000670.2:g.18400712T>C GRCh38
NC_000008.10:g.18258222T>C , CM000670.1:g.18258222T>C GRCh37
NC_000008.9:g.18302502T>C NCBI36
NG_012246.1:g.14468T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.709T>C MANE Select ENSP00000286479.3:p.Phe237Leu
ENST00000286479.3:c.709T>C ENSP00000286479.3:p.Phe237Leu
ENST00000520116.1:c.319T>C ENSP00000428416.1:p.Phe107Leu
NM_000015.2:c.709T>C NP_000006.2:p.Phe237Leu
XM_011544358.1:c.709T>C XP_011542660.1:p.Phe237Leu
XM_017012938.1:c.709T>C XP_016868427.1:p.Phe237Leu
NM_000015.3:c.709T>C MANE Select NP_000006.2:p.Phe237Leu