Canonical Allele Identifier: CA4651591
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs749903527
gnomAD v2: 8-18257821-C-G
gnomAD v4: 8-18400311-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400311C>G , CM000670.2:g.18400311C>G GRCh38
NC_000008.10:g.18257821C>G , CM000670.1:g.18257821C>G GRCh37
NC_000008.9:g.18302101C>G NCBI36
NG_012246.1:g.14067C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.308C>G MANE Select ENSP00000286479.3:p.Thr103Ser
ENST00000286479.3:c.308C>G ENSP00000286479.3:p.Thr103Ser
ENST00000520116.1:c.-57-26C>G ENSP00000428416.1:n.-57-26C>G
NM_000015.2:c.308C>G NP_000006.2:p.Thr103Ser
XM_011544358.1:c.308C>G XP_011542660.1:p.Thr103Ser
XM_017012938.1:c.308C>G XP_016868427.1:p.Thr103Ser
NM_000015.3:c.308C>G MANE Select NP_000006.2:p.Thr103Ser