Canonical Allele Identifier: CA370635434
Gene: NAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.18257740A>G (hg19) chr8:g.18400230A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400230A>G , CM000670.2:g.18400230A>G GRCh38
NC_000008.10:g.18257740A>G , CM000670.1:g.18257740A>G GRCh37
NC_000008.9:g.18302020A>G NCBI36
NG_012246.1:g.13986A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.227A>G MANE Select ENSP00000286479.3:p.Tyr76Cys
ENST00000286479.3:c.227A>G ENSP00000286479.3:p.Tyr76Cys
ENST00000520116.1:c.-57-107A>G ENSP00000428416.1:n.-57-107A>G
NM_000015.2:c.227A>G NP_000006.2:p.Tyr76Cys
XM_011544358.1:c.227A>G XP_011542660.1:p.Tyr76Cys
XM_017012938.1:c.227A>G XP_016868427.1:p.Tyr76Cys
NM_000015.3:c.227A>G MANE Select NP_000006.2:p.Tyr76Cys
Search 100 bp 5'
Search 100 bp 3'