Canonical Allele Identifier: CA459699351
Gene: NAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.18258221C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400711C>G , CM000670.2:g.18400711C>G GRCh38
NC_000008.10:g.18258221C>G , CM000670.1:g.18258221C>G GRCh37
NC_000008.9:g.18302501C>G NCBI36
NG_012246.1:g.14467C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.708C>G MANE Select ENSP00000286479.3:p.Gly236=
ENST00000286479.3:c.708C>G ENSP00000286479.3:p.Gly236=
ENST00000520116.1:c.318C>G ENSP00000428416.1:p.Gly106=
NM_000015.2:c.708C>G NP_000006.2:p.Gly236=
XM_011544358.1:c.708C>G XP_011542660.1:p.Gly236=
XM_017012938.1:c.708C>G XP_016868427.1:p.Gly236=
NM_000015.3:c.708C>G MANE Select NP_000006.2:p.Gly236=