Canonical Allele Identifier: CA2659622929
Gene: NAT8 HGNC NCBI

Linked Data

gnomAD v4: 2-73640910-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73640910T>C , CM000664.2:g.73640910T>C GRCh38
NC_000002.11:g.73868037T>C , CM000664.1:g.73868037T>C GRCh37
NC_000002.10:g.73721545T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272425.4:c.*35A>G MANE Select ENSP00000272425.3:n.*35A>G
ENST00000272425.3:c.*35A>G ENSP00000272425.3:n.*35A>G
NM_003960.3:c.*35A>G NP_003951.3:n.*35A>G
NM_003960.4:c.*35A>G MANE Select NP_003951.3:n.*35A>G