Canonical Allele Identifier: CA4651552
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs377338395
gnomAD v2: 8-18257619-C-G
gnomAD v4: 8-18400109-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400109C>G , CM000670.2:g.18400109C>G GRCh38
NC_000008.10:g.18257619C>G , CM000670.1:g.18257619C>G GRCh37
NC_000008.9:g.18301899C>G NCBI36
NG_012246.1:g.13865C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.106C>G MANE Select ENSP00000286479.3:p.Pro36Ala
ENST00000286479.3:c.106C>G ENSP00000286479.3:p.Pro36Ala
ENST00000520116.1:c.-57-228C>G ENSP00000428416.1:n.-57-228C>G
NM_000015.2:c.106C>G NP_000006.2:p.Pro36Ala
XM_011544358.1:c.106C>G XP_011542660.1:p.Pro36Ala
XM_017012938.1:c.106C>G XP_016868427.1:p.Pro36Ala
NM_000015.3:c.106C>G MANE Select NP_000006.2:p.Pro36Ala