Canonical Allele Identifier: CA4651713
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs772095430
ExAC: 8:18258360 C / G
gnomAD v2: 8-18258360-C-G
gnomAD v3: 8-18400850-C-G
gnomAD v4: 8-18400850-C-G
MyVariant Identifiers: chr8:g.18258360C>G (hg19) chr8:g.18400850C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400850C>G , CM000670.2:g.18400850C>G GRCh38
NC_000008.10:g.18258360C>G , CM000670.1:g.18258360C>G GRCh37
NC_000008.9:g.18302640C>G NCBI36
NG_012246.1:g.14606C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.847C>G MANE Select ENSP00000286479.3:p.Pro283Ala
ENST00000286479.3:c.847C>G ENSP00000286479.3:p.Pro283Ala
ENST00000520116.1:c.457C>G ENSP00000428416.1:p.Pro153Ala
NM_000015.2:c.847C>G NP_000006.2:p.Pro283Ala
XM_011544358.1:c.847C>G XP_011542660.1:p.Pro283Ala
XM_017012938.1:c.847C>G XP_016868427.1:p.Pro283Ala
NM_000015.3:c.847C>G MANE Select NP_000006.2:p.Pro283Ala
Search 100 bp 5'
Search 100 bp 3'