Canonical Allele Identifier: CA370635836
Gene: NAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400422G>C , CM000670.2:g.18400422G>C GRCh38
NC_000008.10:g.18257932G>C , CM000670.1:g.18257932G>C GRCh37
NC_000008.9:g.18302212G>C NCBI36
NG_012246.1:g.14178G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.419G>C MANE Select ENSP00000286479.3:p.Gly140Ala
ENST00000286479.3:c.419G>C ENSP00000286479.3:p.Gly140Ala
ENST00000520116.1:c.29G>C ENSP00000428416.1:p.Gly10Ala
NM_000015.2:c.419G>C NP_000006.2:p.Gly140Ala
XM_011544358.1:c.419G>C XP_011542660.1:p.Gly140Ala
XM_017012938.1:c.419G>C XP_016868427.1:p.Gly140Ala
NM_000015.3:c.419G>C MANE Select NP_000006.2:p.Gly140Ala