Canonical Allele Identifier: CA12831926
Gene: NAT2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs9987109

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18393412T>C , CM000670.2:g.18393412T>C GRCh38
NC_000008.10:g.18250922T>C , CM000670.1:g.18250922T>C GRCh37
NC_000008.9:g.18295202T>C NCBI36
NG_012246.1:g.7168T>C

Transcript Alleles

HGVS Amino-acid change
NM_000015.2:c.-7+2067T>C VV NP_000006.2:p.=
XM_011544358.1:c.-7+676T>C XP_011542660.1:p.=
XM_017012938.1:c.-7+6376T>C XP_016868427.1:p.=
NM_000015.3:c.-7+2067T>C VV MANE Preferred NP_000006.2:p.=
ENST00000286479.3:c.-7+2067T>C ENSP00000286479.3:p.=
ENST00000520116.1:c.-58+2067T>C ENSP00000428416.1:p.=