Canonical Allele Identifier: CA891063851
Gene: PADI2 HGNC NCBI

Linked Data

dbSNP Id: rs1195467809
gnomAD v3: 1-17118355-T-G
gnomAD v4: 1-17118355-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17118355T>G , CM000663.2:g.17118355T>G GRCh38
NC_000001.10:g.17444850T>G , CM000663.1:g.17444850T>G GRCh37
NC_000001.9:g.17317437T>G NCBI36
NG_033958.1:g.6099A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375486.9:c.92+925A>C MANE Select ENSP00000364635.4:n.92+925A>C
ENST00000375481.1:c.92+925A>C ENSP00000364630.1:n.92+925A>C
ENST00000375486.8:c.92+925A>C ENSP00000364635.4:n.92+925A>C
NM_007365.2:c.92+925A>C NP_031391.2:n.92+925A>C
XM_011540549.1:c.92+925A>C XP_011538851.1:n.92+925A>C
XR_947004.1:n.4931T>G
XR_001736944.1:n.174+925A>C
NM_007365.3:c.92+925A>C MANE Select NP_031391.2:n.92+925A>C