Canonical Allele Identifier: CA459700202
Gene: NAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.18258383T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400873T>C , CM000670.2:g.18400873T>C GRCh38
NC_000008.10:g.18258383T>C , CM000670.1:g.18258383T>C GRCh37
NC_000008.9:g.18302663T>C NCBI36
NG_012246.1:g.14629T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.870T>C MANE Select ENSP00000286479.3:p.Ile290=
ENST00000286479.3:c.870T>C ENSP00000286479.3:p.Ile290=
ENST00000520116.1:c.480T>C ENSP00000428416.1:p.Ile160=
NM_000015.2:c.870T>C NP_000006.2:p.Ile290=
XM_011544358.1:c.870T>C XP_011542660.1:p.Ile290=
XM_017012938.1:c.870T>C XP_016868427.1:p.Ile290=
NM_000015.3:c.870T>C MANE Select NP_000006.2:p.Ile290=
Search 100 bp 5'
Search 100 bp 3'