Canonical Allele Identifier: CA347286262

Gene: NAT8

Linked Data

• MyVariant Identifiers: chr2:g.73868130G>A (hg19) ; chr2:g.73641003G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73641003G>A , CM000664.2:g.73641003G>A	GRCh38
NC_000002.11:g.73868130G>A , CM000664.1:g.73868130G>A	GRCh37
NC_000002.10:g.73721638G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272425.4:c.626C>T MANE Select	ENSP00000272425.3:p.Ala209Val
ENST00000272425.3:c.626C>T	ENSP00000272425.3:p.Ala209Val
NM_003960.3:c.626C>T	NP_003951.3:p.Ala209Val
NM_003960.4:c.626C>T MANE Select	NP_003951.3:p.Ala209Val