Canonical Allele Identifier: CA370636411
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1800776439
gnomAD v3: 8-18400688-G-T
gnomAD v4: 8-18400688-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400688G>T , CM000670.2:g.18400688G>T GRCh38
NC_000008.10:g.18258198G>T , CM000670.1:g.18258198G>T GRCh37
NC_000008.9:g.18302478G>T NCBI36
NG_012246.1:g.14444G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.685G>T MANE Select ENSP00000286479.3:p.Glu229Ter
ENST00000286479.3:c.685G>T ENSP00000286479.3:p.Glu229Ter
ENST00000520116.1:c.295G>T ENSP00000428416.1:p.Glu99Ter
NM_000015.2:c.685G>T NP_000006.2:p.Glu229Ter
XM_011544358.1:c.685G>T XP_011542660.1:p.Glu229Ter
XM_017012938.1:c.685G>T XP_016868427.1:p.Glu229Ter
NM_000015.3:c.685G>T MANE Select NP_000006.2:p.Glu229Ter