Canonical Allele Identifier: CA427024343
Gene: NAT8 HGNC NCBI

Linked Data

dbSNP Id: rs1676382266
MyVariant Identifiers: chr2:g.73868140T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73641013T>G , CM000664.2:g.73641013T>G GRCh38
NC_000002.11:g.73868140T>G , CM000664.1:g.73868140T>G GRCh37
NC_000002.10:g.73721648T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272425.4:c.616A>C MANE Select ENSP00000272425.3:p.Arg206=
ENST00000272425.3:c.616A>C ENSP00000272425.3:p.Arg206=
NM_003960.3:c.616A>C NP_003951.3:p.Arg206=
NM_003960.4:c.616A>C MANE Select NP_003951.3:p.Arg206=
Search 100 bp 5'
Search 100 bp 3'