Canonical Allele Identifier: CA18635302
Gene: PADI4 HGNC NCBI

Linked Data

dbSNP Id: rs561478777
gnomAD v4: 1-17333921-T-C
MyVariant Identifiers: chr1:g.17660416T>C (hg19) chr1:g.17333921T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17333921T>C , CM000663.2:g.17333921T>C GRCh38
NC_000001.10:g.17660416T>C , CM000663.1:g.17660416T>C GRCh37
NC_000001.9:g.17533003T>C NCBI36
NG_023261.2:g.30732T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375448.4:c.274-22T>C MANE Select ENSP00000364597.4:n.274-22T>C
ENST00000375453.5:c.274-22T>C ENSP00000364602.1:n.274-22T>C
NM_012387.2:c.274-22T>C NP_036519.2:n.274-22T>C
XM_011541150.1:c.274-22T>C XP_011539452.1:n.274-22T>C
XM_011541151.1:c.274-22T>C XP_011539453.1:n.274-22T>C
XM_011541153.1:c.274-22T>C XP_011539455.1:n.274-22T>C
XM_011541154.1:c.274-22T>C XP_011539456.1:n.274-22T>C
XM_011541155.1:c.274-22T>C XP_011539457.1:n.274-22T>C
XM_011541156.1:c.274-22T>C XP_011539458.1:n.274-22T>C
XM_011541154.2:c.274-22T>C XP_011539456.1:n.274-22T>C
NM_012387.3:c.274-22T>C MANE Select NP_036519.2:n.274-22T>C
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