Canonical Allele Identifier: CA338245778
Gene: PADI6 HGNC NCBI

Linked Data

dbSNP Id: rs1570130275
MyVariant Identifiers: chr1:g.17708542A>C (hg19) chr1:g.17382047A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17382047A>C , CM000663.2:g.17382047A>C GRCh38
NC_000001.10:g.17708542A>C , CM000663.1:g.17708542A>C GRCh37
NC_000001.9:g.17581129A>C NCBI36
NG_032943.1:g.14802A>C
NG_032943.2:g.14802A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000619609.1:c.634A>C MANE Select ENSP00000483125.1:p.Thr212Pro
NM_207421.4:c.634A>C MANE Select NP_997304.3:p.Thr212Pro
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