Canonical Allele Identifier: CA1261057038
Gene: NAT8 HGNC NCBI

Linked Data

dbSNP Id: rs1676378979
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73640886G>C , CM000664.2:g.73640886G>C GRCh38
NC_000002.11:g.73868013G>C , CM000664.1:g.73868013G>C GRCh37
NC_000002.10:g.73721521G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272425.4:c.*59C>G MANE Select ENSP00000272425.3:n.*59C>G
ENST00000272425.3:c.*59C>G ENSP00000272425.3:n.*59C>G
NM_003960.3:c.*59C>G NP_003951.3:n.*59C>G
NM_003960.4:c.*59C>G MANE Select NP_003951.3:n.*59C>G
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