Canonical Allele Identifier: CA891283020
Gene: PADI6 HGNC NCBI

Linked Data

dbSNP Id: rs1300038837
gnomAD v4: 1-17401126-C-T
MyVariant Identifiers: chr1:g.17401126C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17401126C>T , CM000663.2:g.17401126C>T GRCh38
NC_000001.10:g.17727622C>T , CM000663.1:g.17727622C>T GRCh37
NC_000001.9:g.17600209C>T NCBI36
NG_032943.1:g.33881C>T
NG_032943.2:g.33881C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000619609.1:c.1852-79C>T MANE Select ENSP00000483125.1:n.1852-79C>T
NM_207421.4:c.1852-79C>T MANE Select NP_997304.3:n.1852-79C>T
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