Canonical Allele Identifier: CA173519042
Gene: NAT2 HGNC NCBI

Linked Data

dbSNP Id: rs185870259
gnomAD v3: 8-18393426-G-C
gnomAD v4: 8-18393426-G-C
MyVariant Identifiers: chr8:g.18250936G>C (hg19) chr8:g.18393426G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18393426G>C , CM000670.2:g.18393426G>C GRCh38
NC_000008.10:g.18250936G>C , CM000670.1:g.18250936G>C GRCh37
NC_000008.9:g.18295216G>C NCBI36
NG_012246.1:g.7182G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.-7+2081G>C MANE Select ENSP00000286479.3:n.-7+2081G>C
ENST00000286479.3:c.-7+2081G>C ENSP00000286479.3:n.-7+2081G>C
ENST00000520116.1:c.-58+2081G>C ENSP00000428416.1:n.-58+2081G>C
NM_000015.2:c.-7+2081G>C NP_000006.2:n.-7+2081G>C
XM_011544358.1:c.-7+690G>C XP_011542660.1:n.-7+690G>C
XM_017012938.1:c.-7+6390G>C XP_016868427.1:n.-7+6390G>C
NM_000015.3:c.-7+2081G>C MANE Select NP_000006.2:n.-7+2081G>C
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