Canonical Allele Identifier: CA50370914
Gene: NAT8 HGNC NCBI

Linked Data

dbSNP Id: rs35112876
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73640997dup , CM000664.2:g.73640997dup GRCh38
NC_000002.11:g.73868124dup , CM000664.1:g.73868124dup GRCh37
NC_000002.10:g.73721632dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272425.4:c.632dup MANE Select ENSP00000272425.3:p.His211GlnfsTer13
ENST00000272425.3:c.632dup ENSP00000272425.3:p.His211GlnfsTer13
NM_003960.3:c.632dup NP_003951.3:p.His211GlnfsTer13
NM_003960.4:c.632dup MANE Select NP_003951.3:p.His211GlnfsTer13
Search 100 bp 5'
Search 100 bp 3'