Canonical Allele Identifier: CA370635461
Gene: NAT2 HGNC NCBI

Linked Data

gnomAD v4: 8-18400242-C-A
MyVariant Identifiers: chr8:g.18257752C>A (hg19) chr8:g.18400242C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400242C>A , CM000670.2:g.18400242C>A GRCh38
NC_000008.10:g.18257752C>A , CM000670.1:g.18257752C>A GRCh37
NC_000008.9:g.18302032C>A NCBI36
NG_012246.1:g.13998C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.239C>A MANE Select ENSP00000286479.3:p.Thr80Asn
ENST00000286479.3:c.239C>A ENSP00000286479.3:p.Thr80Asn
ENST00000520116.1:c.-57-95C>A ENSP00000428416.1:n.-57-95C>A
NM_000015.2:c.239C>A NP_000006.2:p.Thr80Asn
XM_011544358.1:c.239C>A XP_011542660.1:p.Thr80Asn
XM_017012938.1:c.239C>A XP_016868427.1:p.Thr80Asn
NM_000015.3:c.239C>A MANE Select NP_000006.2:p.Thr80Asn
Search 100 bp 5'
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