Canonical Allele Identifier: CA641680
Gene: PADI6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3036080
ClinVar RCV Id: RCV003897417
dbSNP Id: rs767987621
ExAC: 1:17720787 C / A
gnomAD v2: 1-17720787-C-A
gnomAD v3: 1-17394291-C-A
gnomAD v4: 1-17394291-C-A
MyVariant Identifiers: chr1:g.17720787C>A (hg19) chr1:g.17394291C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17394291C>A , CM000663.2:g.17394291C>A GRCh38
NC_000001.10:g.17720787C>A , CM000663.1:g.17720787C>A GRCh37
NC_000001.9:g.17593374C>A NCBI36
NG_032943.1:g.27046C>A
NG_032943.2:g.27046C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000619609.1:c.1183-9C>A MANE Select ENSP00000483125.1:n.1183-9C>A
NM_207421.4:c.1183-9C>A MANE Select NP_997304.3:n.1183-9C>A
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