Canonical Allele Identifier: CA4651656
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs750343726
gnomAD v2: 8-18258114-G-A
gnomAD v4: 8-18400604-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400604G>A , CM000670.2:g.18400604G>A GRCh38
NC_000008.10:g.18258114G>A , CM000670.1:g.18258114G>A GRCh37
NC_000008.9:g.18302394G>A NCBI36
NG_012246.1:g.14360G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.601G>A MANE Select ENSP00000286479.3:p.Asp201Asn
ENST00000286479.3:c.601G>A ENSP00000286479.3:p.Asp201Asn
ENST00000520116.1:c.211G>A ENSP00000428416.1:p.Asp71Asn
NM_000015.2:c.601G>A NP_000006.2:p.Asp201Asn
XM_011544358.1:c.601G>A XP_011542660.1:p.Asp201Asn
XM_017012938.1:c.601G>A XP_016868427.1:p.Asp201Asn
NM_000015.3:c.601G>A MANE Select NP_000006.2:p.Asp201Asn