Canonical Allele Identifier: CA459699334
Gene: NAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.18258218G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400708G>C , CM000670.2:g.18400708G>C GRCh38
NC_000008.10:g.18258218G>C , CM000670.1:g.18258218G>C GRCh37
NC_000008.9:g.18302498G>C NCBI36
NG_012246.1:g.14464G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.705G>C MANE Select ENSP00000286479.3:p.Val235=
ENST00000286479.3:c.705G>C ENSP00000286479.3:p.Val235=
ENST00000520116.1:c.315G>C ENSP00000428416.1:p.Val105=
NM_000015.2:c.705G>C NP_000006.2:p.Val235=
XM_011544358.1:c.705G>C XP_011542660.1:p.Val235=
XM_017012938.1:c.705G>C XP_016868427.1:p.Val235=
NM_000015.3:c.705G>C MANE Select NP_000006.2:p.Val235=