Canonical Allele Identifier: CA370635984
Gene: NAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400488A>G , CM000670.2:g.18400488A>G GRCh38
NC_000008.10:g.18257998A>G , CM000670.1:g.18257998A>G GRCh37
NC_000008.9:g.18302278A>G NCBI36
NG_012246.1:g.14244A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.485A>G MANE Select ENSP00000286479.3:p.Asp162Gly
ENST00000286479.3:c.485A>G ENSP00000286479.3:p.Asp162Gly
ENST00000520116.1:c.95A>G ENSP00000428416.1:p.Asp32Gly
NM_000015.2:c.485A>G NP_000006.2:p.Asp162Gly
XM_011544358.1:c.485A>G XP_011542660.1:p.Asp162Gly
XM_017012938.1:c.485A>G XP_016868427.1:p.Asp162Gly
NM_000015.3:c.485A>G MANE Select NP_000006.2:p.Asp162Gly