Canonical Allele Identifier: CA891285819
Gene: PADI6 HGNC NCBI

Linked Data

dbSNP Id: rs1292790770
gnomAD v4: 1-17381911-C-T
MyVariant Identifiers: chr1:g.17381911C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17381911C>T , CM000663.2:g.17381911C>T GRCh38
NC_000001.10:g.17708406C>T , CM000663.1:g.17708406C>T GRCh37
NC_000001.9:g.17580993C>T NCBI36
NG_032943.1:g.14666C>T
NG_032943.2:g.14666C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000619609.1:c.554-56C>T MANE Select ENSP00000483125.1:n.554-56C>T
NM_207421.4:c.554-56C>T MANE Select NP_997304.3:n.554-56C>T
Search 100 bp 5'
Search 100 bp 3'