Canonical Allele Identifier: CA2686326478
Gene: NAT2 HGNC NCBI

Linked Data

gnomAD v4: 8-18400942-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400942A>G , CM000670.2:g.18400942A>G GRCh38
NC_000008.10:g.18258452A>G , CM000670.1:g.18258452A>G GRCh37
NC_000008.9:g.18302732A>G NCBI36
NG_012246.1:g.14698A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.*66A>G MANE Select ENSP00000286479.3:n.*66A>G
ENST00000286479.3:c.*66A>G ENSP00000286479.3:n.*66A>G
ENST00000520116.1:c.*66A>G ENSP00000428416.1:n.*66A>G
NM_000015.2:c.*66A>G NP_000006.2:n.*66A>G
XM_011544358.1:c.*66A>G XP_011542660.1:n.*66A>G
XM_017012938.1:c.*66A>G XP_016868427.1:n.*66A>G
NM_000015.3:c.*66A>G MANE Select NP_000006.2:n.*66A>G
Search 100 bp 5'
Search 100 bp 3'