Canonical Allele Identifier: CA459699263
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs111750824
gnomAD v2: 8-18257661-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400151T>C , CM000670.2:g.18400151T>C GRCh38
NC_000008.10:g.18257661T>C , CM000670.1:g.18257661T>C GRCh37
NC_000008.9:g.18301941T>C NCBI36
NG_012246.1:g.13907T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.148T>C MANE Select ENSP00000286479.3:p.Leu50=
ENST00000286479.3:c.148T>C ENSP00000286479.3:p.Leu50=
ENST00000520116.1:c.-57-186T>C ENSP00000428416.1:n.-57-186T>C
NM_000015.2:c.148T>C NP_000006.2:p.Leu50=
XM_011544358.1:c.148T>C XP_011542660.1:p.Leu50=
XM_017012938.1:c.148T>C XP_016868427.1:p.Leu50=
NM_000015.3:c.148T>C MANE Select NP_000006.2:p.Leu50=