Canonical Allele Identifier: CA521046348
Gene: PADI6 HGNC NCBI

Linked Data

dbSNP Id: rs1191411561
gnomAD v2: 1-17720616-A-G
gnomAD v4: 1-17394120-A-G
MyVariant Identifiers: chr1:g.17720616_17720618delinsGTC (hg19) chr1:g.17394120_17394122delinsGTC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17394120A>G , CM000663.2:g.17394120A>G GRCh38
NC_000001.10:g.17720616A>G , CM000663.1:g.17720616A>G GRCh37
NC_000001.9:g.17593203A>G NCBI36
NG_032943.1:g.26875A>G
NG_032943.2:g.26875A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000619609.1:c.1182+38A>G MANE Select ENSP00000483125.1:n.1182+38A>G
NM_207421.4:c.1182+38A>G MANE Select NP_997304.3:n.1182+38A>G
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