Canonical Allele Identifier: CA18660792
Gene: PADI6 HGNC NCBI

Linked Data

dbSNP Id: rs930804784
MyVariant Identifiers: chr1:g.17401026A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17401026A>T , CM000663.2:g.17401026A>T GRCh38
NC_000001.10:g.17727522A>T , CM000663.1:g.17727522A>T GRCh37
NC_000001.9:g.17600109A>T NCBI36
NG_032943.1:g.33781A>T
NG_032943.2:g.33781A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000619609.1:c.1852-179A>T MANE Select ENSP00000483125.1:n.1852-179A>T
NM_207421.4:c.1852-179A>T MANE Select NP_997304.3:n.1852-179A>T
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