Canonical Allele Identifier: CA18648613
Gene: PADI6 HGNC NCBI

Linked Data

dbSNP Id: rs532914694
gnomAD v4: 1-17394317-C-T
MyVariant Identifiers: chr1:g.17720813C>T (hg19) chr1:g.17394317C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17394317C>T , CM000663.2:g.17394317C>T GRCh38
NC_000001.10:g.17720813C>T , CM000663.1:g.17720813C>T GRCh37
NC_000001.9:g.17593400C>T NCBI36
NG_032943.1:g.27072C>T
NG_032943.2:g.27072C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000619609.1:c.1200C>T MANE Select ENSP00000483125.1:p.Tyr400=
NM_207421.4:c.1200C>T MANE Select NP_997304.3:p.Tyr400=
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