Canonical Allele Identifier: CA641667
Gene: PADI6 HGNC NCBI

Linked Data

dbSNP Id: rs10458537
ExAC: 1:17720615 A / C
gnomAD v2: 1-17720615-A-C
gnomAD v3: 1-17394119-A-C
gnomAD v4: 1-17394119-A-C
MyVariant Identifiers: chr1:g.17720615A>C (hg19) chr1:g.17394119A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17394119A>C , CM000663.2:g.17394119A>C GRCh38
NC_000001.10:g.17720615A>C , CM000663.1:g.17720615A>C GRCh37
NC_000001.9:g.17593202A>C NCBI36
NG_032943.1:g.26874A>C
NG_032943.2:g.26874A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000619609.1:c.1182+37A>C MANE Select ENSP00000483125.1:n.1182+37A>C
NM_207421.4:c.1182+37A>C MANE Select NP_997304.3:n.1182+37A>C
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