Canonical Allele Identifier: CA891285707
Gene: PADI6 HGNC NCBI

Linked Data

dbSNP Id: rs1207605159
MyVariant Identifiers: chr1:g.17381771C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17381771C>T , CM000663.2:g.17381771C>T GRCh38
NC_000001.10:g.17708266C>T , CM000663.1:g.17708266C>T GRCh37
NC_000001.9:g.17580853C>T NCBI36
NG_032943.1:g.14526C>T
NG_032943.2:g.14526C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000619609.1:c.554-196C>T MANE Select ENSP00000483125.1:n.554-196C>T
NM_207421.4:c.554-196C>T MANE Select NP_997304.3:n.554-196C>T