Canonical Allele Identifier: CA338255278
Gene: PADI6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1308684
ClinVar RCV Id: RCV001814594
dbSNP Id: rs2100316108
MyVariant Identifiers: chr1:g.17392157A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17392157A>C , CM000663.2:g.17392157A>C GRCh38
NG_032943.1:g.24912A>C
NG_032943.2:g.24912A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000619609.1:c.1006A>C MANE Select ENSP00000483125.1:p.Ser336Arg
NM_207421.4:c.1006A>C MANE Select NP_997304.3:p.Ser336Arg
Search 100 bp 5'
Search 100 bp 3'