Canonical Allele Identifier: CA18621828
Gene: PADI2 HGNC NCBI

Linked Data

dbSNP Id: rs558299629
MyVariant Identifiers: chr1:g.17444630T>G (hg19) chr1:g.17118135T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17118135T>G , CM000663.2:g.17118135T>G GRCh38
NC_000001.10:g.17444630T>G , CM000663.1:g.17444630T>G GRCh37
NC_000001.9:g.17317217T>G NCBI36
NG_033958.1:g.6319A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375486.9:c.92+1145A>C MANE Select ENSP00000364635.4:n.92+1145A>C
ENST00000375481.1:c.92+1145A>C ENSP00000364630.1:n.92+1145A>C
ENST00000375486.8:c.92+1145A>C ENSP00000364635.4:n.92+1145A>C
NM_007365.2:c.92+1145A>C NP_031391.2:n.92+1145A>C
XM_011540549.1:c.92+1145A>C XP_011538851.1:n.92+1145A>C
XR_947004.1:n.4711T>G
XR_001736944.1:n.174+1145A>C
NM_007365.3:c.92+1145A>C MANE Select NP_031391.2:n.92+1145A>C
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