Canonical Allele Identifier: CA416409141
Gene: PADI6 HGNC NCBI

Linked Data

dbSNP Id: rs2075302551
gnomAD v4: 1-17401632-A-C
MyVariant Identifiers: chr1:g.17728128A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17401632A>C , CM000663.2:g.17401632A>C GRCh38
NC_000001.10:g.17728128A>C , CM000663.1:g.17728128A>C GRCh37
NC_000001.9:g.17600715A>C NCBI36
NG_032943.1:g.34387A>C
NG_032943.2:g.34387A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000619609.1:c.*194A>C MANE Select ENSP00000483125.1:n.*194A>C
NM_207421.4:c.*194A>C MANE Select NP_997304.3:n.*194A>C
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