Canonical Allele Identifier: CA1768215614
Gene: NAT2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18393706A= , CM000670.2:g.18393706A= GRCh38
NC_000008.10:g.18251216A= , CM000670.1:g.18251216A= GRCh37
NC_000008.9:g.18295496A= NCBI36
NG_012246.1:g.7462A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.-7+2361A= MANE Select ENSP00000286479.3:n.-7+2361A=
ENST00000286479.3:c.-7+2361A= ENSP00000286479.3:n.-7+2361A=
ENST00000520116.1:c.-58+2361A= ENSP00000428416.1:n.-58+2361A=
NM_000015.2:c.-7+2361A= NP_000006.2:n.-7+2361A=
XM_011544358.1:c.-7+970A= XP_011542660.1:n.-7+970A=
XM_017012938.1:c.-6-6292A= XP_016868427.1:n.-6-6292A=
NM_000015.3:c.-7+2361A= MANE Select NP_000006.2:n.-7+2361A=
Search 100 bp 5'
Search 100 bp 3'