Canonical Allele Identifier: CA4651644
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs769102650
gnomAD v2: 8-18258083-C-T
gnomAD v4: 8-18400573-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400573C>T , CM000670.2:g.18400573C>T GRCh38
NC_000008.10:g.18258083C>T , CM000670.1:g.18258083C>T GRCh37
NC_000008.9:g.18302363C>T NCBI36
NG_012246.1:g.14329C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.570C>T MANE Select ENSP00000286479.3:p.Tyr190=
ENST00000286479.3:c.570C>T ENSP00000286479.3:p.Tyr190=
ENST00000520116.1:c.180C>T ENSP00000428416.1:p.Tyr60=
NM_000015.2:c.570C>T NP_000006.2:p.Tyr190=
XM_011544358.1:c.570C>T XP_011542660.1:p.Tyr190=
XM_017012938.1:c.570C>T XP_016868427.1:p.Tyr190=
NM_000015.3:c.570C>T MANE Select NP_000006.2:p.Tyr190=