Canonical Allele Identifier: CA641688
Gene: PADI6 HGNC NCBI

Linked Data

dbSNP Id: rs755798854
ExAC: 1:17720825 C / T
gnomAD v2: 1-17720825-C-T
gnomAD v4: 1-17394329-C-T
MyVariant Identifiers: chr1:g.17720825C>T (hg19) chr1:g.17394329C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17394329C>T , CM000663.2:g.17394329C>T GRCh38
NC_000001.10:g.17720825C>T , CM000663.1:g.17720825C>T GRCh37
NC_000001.9:g.17593412C>T NCBI36
NG_032943.1:g.27084C>T
NG_032943.2:g.27084C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000619609.1:c.1212C>T MANE Select ENSP00000483125.1:p.Asp404=
NM_207421.4:c.1212C>T MANE Select NP_997304.3:p.Asp404=
Search 100 bp 5'
Search 100 bp 3'