Canonical Allele Identifier: CA4651548
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs763283305
gnomAD v2: 8-18257610-C-T
gnomAD v3: 8-18400100-C-T
gnomAD v4: 8-18400100-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400100C>T , CM000670.2:g.18400100C>T GRCh38
NC_000008.10:g.18257610C>T , CM000670.1:g.18257610C>T GRCh37
NC_000008.9:g.18301890C>T NCBI36
NG_012246.1:g.13856C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.97C>T MANE Select ENSP00000286479.3:p.Arg33Trp
ENST00000286479.3:c.97C>T ENSP00000286479.3:p.Arg33Trp
ENST00000520116.1:c.-57-237C>T ENSP00000428416.1:n.-57-237C>T
NM_000015.2:c.97C>T NP_000006.2:p.Arg33Trp
XM_011544358.1:c.97C>T XP_011542660.1:p.Arg33Trp
XM_017012938.1:c.97C>T XP_016868427.1:p.Arg33Trp
NM_000015.3:c.97C>T MANE Select NP_000006.2:p.Arg33Trp