Canonical Allele Identifier: CA50370748
Gene: NAT8 HGNC NCBI

Linked Data

dbSNP Id: rs35176564
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73640797del , CM000664.2:g.73640797del GRCh38
NC_000002.11:g.73867924del , CM000664.1:g.73867924del GRCh37
NC_000002.10:g.73721432del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272425.4:c.*149del MANE Select ENSP00000272425.3:n.*149del
NM_003960.3:c.*149del NP_003951.3:n.*149del
NM_003960.4:c.*149del MANE Select NP_003951.3:n.*149del
Search 100 bp 5'
Search 100 bp 3'