Canonical Allele Identifier: CA1768215379
Gene: NAT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18393222T= , CM000670.2:g.18393222T= GRCh38
NC_000008.10:g.18250732T= , CM000670.1:g.18250732T= GRCh37
NC_000008.9:g.18295012T= NCBI36
NG_012246.1:g.6978T=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.-7+1877T= MANE Select ENSP00000286479.3:n.-7+1877T=
ENST00000286479.3:c.-7+1877T= ENSP00000286479.3:n.-7+1877T=
ENST00000520116.1:c.-58+1877T= ENSP00000428416.1:n.-58+1877T=
NM_000015.2:c.-7+1877T= NP_000006.2:n.-7+1877T=
XM_011544358.1:c.-7+486T= XP_011542660.1:n.-7+486T=
XM_017012938.1:c.-7+6186T= XP_016868427.1:n.-7+6186T=
NM_000015.3:c.-7+1877T= MANE Select NP_000006.2:n.-7+1877T=
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