Canonical Allele Identifier: CA1768215491
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1800622979

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18393441A>G , CM000670.2:g.18393441A>G GRCh38
NC_000008.10:g.18250951A>G , CM000670.1:g.18250951A>G GRCh37
NC_000008.9:g.18295231A>G NCBI36
NG_012246.1:g.7197A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.-7+2096A>G MANE Select ENSP00000286479.3:n.-7+2096A>G
ENST00000286479.3:c.-7+2096A>G ENSP00000286479.3:n.-7+2096A>G
ENST00000520116.1:c.-58+2096A>G ENSP00000428416.1:n.-58+2096A>G
NM_000015.2:c.-7+2096A>G NP_000006.2:n.-7+2096A>G
XM_011544358.1:c.-7+705A>G XP_011542660.1:n.-7+705A>G
XM_017012938.1:c.-7+6405A>G XP_016868427.1:n.-7+6405A>G
NM_000015.3:c.-7+2096A>G MANE Select NP_000006.2:n.-7+2096A>G