Canonical Allele Identifier: CA370635886
Gene: NAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400445T>G , CM000670.2:g.18400445T>G GRCh38
NC_000008.10:g.18257955T>G , CM000670.1:g.18257955T>G GRCh37
NC_000008.9:g.18302235T>G NCBI36
NG_012246.1:g.14201T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.442T>G MANE Select ENSP00000286479.3:p.Cys148Gly
ENST00000286479.3:c.442T>G ENSP00000286479.3:p.Cys148Gly
ENST00000520116.1:c.52T>G ENSP00000428416.1:p.Cys18Gly
NM_000015.2:c.442T>G NP_000006.2:p.Cys148Gly
XM_011544358.1:c.442T>G XP_011542660.1:p.Cys148Gly
XM_017012938.1:c.442T>G XP_016868427.1:p.Cys148Gly
NM_000015.3:c.442T>G MANE Select NP_000006.2:p.Cys148Gly