Canonical Allele Identifier: CA16042251
Gene: PADI6 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 372228
ClinVar RCV Id: RCV000412544
dbSNP Id: rs1057517681

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17394041C>T , CM000663.2:g.17394041C>T GRCh38
NC_000001.10:g.17720537C>T , CM000663.1:g.17720537C>T GRCh37
NC_000001.9:g.17593124C>T NCBI36
NG_032943.1:g.26796C>T
NG_032943.2:g.26796C>T

Transcript Alleles

HGVS Amino-acid change
NM_207421.4:c.1141C>T VV NP_997304.3:p.Gln381Ter
ENST00000619609.1:c.1141C>T ENSP00000483125.1:p.Gln381Ter