Canonical Allele Identifier: CA892866964

Gene: NAT8

Linked Data

• dbSNP Id: rs1394022329
• MyVariant Identifiers: chr2:g.73868068G>T (hg19) ; chr2:g.73640941G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73640941G>T , CM000664.2:g.73640941G>T	GRCh38
NC_000002.11:g.73868068G>T , CM000664.1:g.73868068G>T	GRCh37
NC_000002.10:g.73721576G>T	NCBI36

Transcript Alleles

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