Canonical Allele Identifier: CA1768215599
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1800630966
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18393679C>A , CM000670.2:g.18393679C>A GRCh38
NC_000008.10:g.18251189C>A , CM000670.1:g.18251189C>A GRCh37
NC_000008.9:g.18295469C>A NCBI36
NG_012246.1:g.7435C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.-7+2334C>A MANE Select ENSP00000286479.3:n.-7+2334C>A
ENST00000286479.3:c.-7+2334C>A ENSP00000286479.3:n.-7+2334C>A
ENST00000520116.1:c.-58+2334C>A ENSP00000428416.1:n.-58+2334C>A
NM_000015.2:c.-7+2334C>A NP_000006.2:n.-7+2334C>A
XM_011544358.1:c.-7+943C>A XP_011542660.1:n.-7+943C>A
XM_017012938.1:c.-6-6319C>A XP_016868427.1:n.-6-6319C>A
NM_000015.3:c.-7+2334C>A MANE Select NP_000006.2:n.-7+2334C>A
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