Canonical Allele Identifier: CA4651582
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs773321494
gnomAD v2: 8-18257764-T-A
gnomAD v4: 8-18400254-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400254T>A , CM000670.2:g.18400254T>A GRCh38
NC_000008.10:g.18257764T>A , CM000670.1:g.18257764T>A GRCh37
NC_000008.9:g.18302044T>A NCBI36
NG_012246.1:g.14010T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.251T>A MANE Select ENSP00000286479.3:p.Phe84Tyr
ENST00000286479.3:c.251T>A ENSP00000286479.3:p.Phe84Tyr
ENST00000520116.1:c.-57-83T>A ENSP00000428416.1:n.-57-83T>A
NM_000015.2:c.251T>A NP_000006.2:p.Phe84Tyr
XM_011544358.1:c.251T>A XP_011542660.1:p.Phe84Tyr
XM_017012938.1:c.251T>A XP_016868427.1:p.Phe84Tyr
NM_000015.3:c.251T>A MANE Select NP_000006.2:p.Phe84Tyr