Canonical Allele Identifier: CA50371455
Gene: NAT8 HGNC NCBI
ALMS1P1 HGNC NCBI

Linked Data

dbSNP Id: rs749134012
gnomAD v4: 2-73641320-A-G
MyVariant Identifiers: chr2:g.73868447A>G (hg19) chr2:g.73641320A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73641320A>G , CM000664.2:g.73641320A>G GRCh38
NC_000002.11:g.73868447A>G , CM000664.1:g.73868447A>G GRCh37
NC_000002.10:g.73721955A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272425.4:c.309T>C (NAT8) MANE Select ENSP00000272425.3:p.Ser103=
ENST00000652439.1:n.238A>G (ALMS1P1)
ENST00000272425.3:c.309T>C (NAT8) ENSP00000272425.3:p.Ser103=
NM_003960.3:c.309T>C (NAT8) NP_003951.3:p.Ser103=
NM_003960.4:c.309T>C (NAT8) MANE Select NP_003951.3:p.Ser103=
Search 100 bp 5'
Search 100 bp 3'