Canonical Allele Identifier: CA1111451062
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1800620738
gnomAD v3: 8-18393333-C-G
gnomAD v4: 8-18393333-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18393333C>G , CM000670.2:g.18393333C>G GRCh38
NC_000008.10:g.18250843C>G , CM000670.1:g.18250843C>G GRCh37
NC_000008.9:g.18295123C>G NCBI36
NG_012246.1:g.7089C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.-7+1988C>G MANE Select ENSP00000286479.3:n.-7+1988C>G
ENST00000286479.3:c.-7+1988C>G ENSP00000286479.3:n.-7+1988C>G
ENST00000520116.1:c.-58+1988C>G ENSP00000428416.1:n.-58+1988C>G
NM_000015.2:c.-7+1988C>G NP_000006.2:n.-7+1988C>G
XM_011544358.1:c.-7+597C>G XP_011542660.1:n.-7+597C>G
XM_017012938.1:c.-7+6297C>G XP_016868427.1:n.-7+6297C>G
NM_000015.3:c.-7+1988C>G MANE Select NP_000006.2:n.-7+1988C>G