Canonical Allele Identifier: CA18641450
Gene: PADI3 HGNC NCBI

Linked Data

dbSNP Id: rs911999694
gnomAD v3: 1-17265098-C-G
gnomAD v4: 1-17265098-C-G
MyVariant Identifiers: chr1:g.17265098C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17265098C>G , CM000663.2:g.17265098C>G GRCh38
NC_000001.10:g.17591593C>G , CM000663.1:g.17591593C>G GRCh37
NC_000001.9:g.17464180C>G NCBI36
NG_052788.1:g.21020C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375460.3:c.347-561C>G MANE Select ENSP00000364609.3:n.347-561C>G
NM_016233.2:c.347-561C>G MANE Select NP_057317.2:n.347-561C>G
XM_006710684.2:c.233-561C>G XP_006710747.1:n.233-561C>G
XM_011541571.1:c.233-561C>G XP_011539873.1:n.233-561C>G
XM_011541572.1:c.347-561C>G XP_011539874.1:n.347-561C>G
XM_011541571.2:c.233-561C>G XP_011539873.1:n.233-561C>G
XM_011541572.2:c.347-561C>G XP_011539874.1:n.347-561C>G