Canonical Allele Identifier: CA4651568
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs779910396
gnomAD v2: 8-18257701-A-G
gnomAD v3: 8-18400191-A-G
gnomAD v4: 8-18400191-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400191A>G , CM000670.2:g.18400191A>G GRCh38
NC_000008.10:g.18257701A>G , CM000670.1:g.18257701A>G GRCh37
NC_000008.9:g.18301981A>G NCBI36
NG_012246.1:g.13947A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.188A>G MANE Select ENSP00000286479.3:p.Asn63Ser
ENST00000286479.3:c.188A>G ENSP00000286479.3:p.Asn63Ser
ENST00000520116.1:c.-57-146A>G ENSP00000428416.1:n.-57-146A>G
NM_000015.2:c.188A>G NP_000006.2:p.Asn63Ser
XM_011544358.1:c.188A>G XP_011542660.1:p.Asn63Ser
XM_017012938.1:c.188A>G XP_016868427.1:p.Asn63Ser
NM_000015.3:c.188A>G MANE Select NP_000006.2:p.Asn63Ser