Canonical Allele Identifier: CA370636031
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1341104335
gnomAD v2: 8-18258018-T-G
gnomAD v4: 8-18400508-T-G
MyVariant Identifiers: chr8:g.18258018T>G (hg19) chr8:g.18400508T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400508T>G , CM000670.2:g.18400508T>G GRCh38
NC_000008.10:g.18258018T>G , CM000670.1:g.18258018T>G GRCh37
NC_000008.9:g.18302298T>G NCBI36
NG_012246.1:g.14264T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.505T>G MANE Select ENSP00000286479.3:p.Tyr169Asp
ENST00000286479.3:c.505T>G ENSP00000286479.3:p.Tyr169Asp
ENST00000520116.1:c.115T>G ENSP00000428416.1:p.Tyr39Asp
NM_000015.2:c.505T>G NP_000006.2:p.Tyr169Asp
XM_011544358.1:c.505T>G XP_011542660.1:p.Tyr169Asp
XM_017012938.1:c.505T>G XP_016868427.1:p.Tyr169Asp
NM_000015.3:c.505T>G MANE Select NP_000006.2:p.Tyr169Asp
Search 100 bp 5'
Search 100 bp 3'