Canonical Allele Identifier: CA370636672
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1235991376
gnomAD v2: 8-18258323-A-G
gnomAD v4: 8-18400813-A-G
MyVariant Identifiers: chr8:g.18258323A>G (hg19) chr8:g.18400813A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400813A>G , CM000670.2:g.18400813A>G GRCh38
NC_000008.10:g.18258323A>G , CM000670.1:g.18258323A>G GRCh37
NC_000008.9:g.18302603A>G NCBI36
NG_012246.1:g.14569A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.810A>G MANE Select ENSP00000286479.3:p.Ile270Met
ENST00000286479.3:c.810A>G ENSP00000286479.3:p.Ile270Met
ENST00000520116.1:c.420A>G ENSP00000428416.1:p.Ile140Met
NM_000015.2:c.810A>G NP_000006.2:p.Ile270Met
XM_011544358.1:c.810A>G XP_011542660.1:p.Ile270Met
XM_017012938.1:c.810A>G XP_016868427.1:p.Ile270Met
NM_000015.3:c.810A>G MANE Select NP_000006.2:p.Ile270Met
Search 100 bp 5'
Search 100 bp 3'