Canonical Allele Identifier: CA892866918
Gene: NAT8 HGNC NCBI

Linked Data

dbSNP Id: rs1429005215
MyVariant Identifiers: chr2:g.73867959T>A (hg19) chr2:g.73640832T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73640832T>A , CM000664.2:g.73640832T>A GRCh38
NC_000002.11:g.73867959T>A , CM000664.1:g.73867959T>A GRCh37
NC_000002.10:g.73721467T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272425.4:c.*113A>T MANE Select ENSP00000272425.3:n.*113A>T
ENST00000272425.3:c.*113A>T ENSP00000272425.3:n.*113A>T
NM_003960.3:c.*113A>T NP_003951.3:n.*113A>T
NM_003960.4:c.*113A>T MANE Select NP_003951.3:n.*113A>T
Search 100 bp 5'
Search 100 bp 3'