Canonical Allele Identifier: CA416405598
Gene: PADI6 HGNC NCBI

Linked Data

gnomAD v4: 1-17395569-T-C
MyVariant Identifiers: chr1:g.17722065T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17395569T>C , CM000663.2:g.17395569T>C GRCh38
NC_000001.10:g.17722065T>C , CM000663.1:g.17722065T>C GRCh37
NC_000001.9:g.17594652T>C NCBI36
NG_032943.1:g.28324T>C
NG_032943.2:g.28324T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000619609.1:c.1524T>C MANE Select ENSP00000483125.1:p.Ser508=
NM_207421.4:c.1524T>C MANE Select NP_997304.3:p.Ser508=
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