Canonical Allele Identifier: CA370636054
Gene: NAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.18258029C>A (hg19) chr8:g.18400519C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400519C>A , CM000670.2:g.18400519C>A GRCh38
NC_000008.10:g.18258029C>A , CM000670.1:g.18258029C>A GRCh37
NC_000008.9:g.18302309C>A NCBI36
NG_012246.1:g.14275C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.516C>A MANE Select ENSP00000286479.3:p.Asn172Lys
ENST00000286479.3:c.516C>A ENSP00000286479.3:p.Asn172Lys
ENST00000520116.1:c.126C>A ENSP00000428416.1:p.Asn42Lys
NM_000015.2:c.516C>A NP_000006.2:p.Asn172Lys
XM_011544358.1:c.516C>A XP_011542660.1:p.Asn172Lys
XM_017012938.1:c.516C>A XP_016868427.1:p.Asn172Lys
NM_000015.3:c.516C>A MANE Select NP_000006.2:p.Asn172Lys
Search 100 bp 5'
Search 100 bp 3'