Canonical Allele Identifier: CA338269032
Gene: PADI6 HGNC NCBI

Linked Data

gnomAD v4: 1-17401311-C-G
MyVariant Identifiers: chr1:g.17727807C>G (hg19) chr1:g.17401311C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17401311C>G , CM000663.2:g.17401311C>G GRCh38
NC_000001.10:g.17727807C>G , CM000663.1:g.17727807C>G GRCh37
NC_000001.9:g.17600394C>G NCBI36
NG_032943.1:g.34066C>G
NG_032943.2:g.34066C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000619609.1:c.1958C>G MANE Select ENSP00000483125.1:p.Pro653Arg
NM_207421.4:c.1958C>G MANE Select NP_997304.3:p.Pro653Arg
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