Canonical Allele Identifier: CA1261056990
Gene: NAT8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73640807C= , CM000664.2:g.73640807C= GRCh38
NC_000002.11:g.73867934C= , CM000664.1:g.73867934C= GRCh37
NC_000002.10:g.73721442C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272425.4:c.*138G= MANE Select ENSP00000272425.3:n.*138G=
NM_003960.3:c.*138G= NP_003951.3:n.*138G=
NM_003960.4:c.*138G= MANE Select NP_003951.3:n.*138G=
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