Canonical Allele Identifier: CA370635062
Gene: NAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.18257568T>A (hg19) chr8:g.18400058T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400058T>A , CM000670.2:g.18400058T>A GRCh38
NC_000008.10:g.18257568T>A , CM000670.1:g.18257568T>A GRCh37
NC_000008.9:g.18301848T>A NCBI36
NG_012246.1:g.13814T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.55T>A MANE Select ENSP00000286479.3:p.Leu19Met
ENST00000286479.3:c.55T>A ENSP00000286479.3:p.Leu19Met
ENST00000520116.1:c.-57-279T>A ENSP00000428416.1:n.-57-279T>A
NM_000015.2:c.55T>A NP_000006.2:p.Leu19Met
XM_011544358.1:c.55T>A XP_011542660.1:p.Leu19Met
XM_017012938.1:c.55T>A XP_016868427.1:p.Leu19Met
NM_000015.3:c.55T>A MANE Select NP_000006.2:p.Leu19Met
Search 100 bp 5'
Search 100 bp 3'