Canonical Allele Identifier: CA641690
Gene: PADI6 HGNC NCBI

Linked Data

dbSNP Id: rs749170626
ExAC: 1:17720828 T / A
gnomAD v2: 1-17720828-T-A
MyVariant Identifiers: chr1:g.17720828T>A (hg19) chr1:g.17394332T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17394332T>A , CM000663.2:g.17394332T>A GRCh38
NC_000001.10:g.17720828T>A , CM000663.1:g.17720828T>A GRCh37
NC_000001.9:g.17593415T>A NCBI36
NG_032943.1:g.27087T>A
NG_032943.2:g.27087T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000619609.1:c.1215T>A MANE Select ENSP00000483125.1:p.Thr405=
NM_207421.4:c.1215T>A MANE Select NP_997304.3:p.Thr405=
Search 100 bp 5'
Search 100 bp 3'