Canonical Allele Identifier: CA891296155
Gene: PADI6 HGNC NCBI

Linked Data

dbSNP Id: rs1160079394
MyVariant Identifiers: chr1:g.17395837A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17395837A>G , CM000663.2:g.17395837A>G GRCh38
NC_000001.10:g.17722333A>G , CM000663.1:g.17722333A>G GRCh37
NC_000001.9:g.17594920A>G NCBI36
NG_032943.1:g.28592A>G
NG_032943.2:g.28592A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000619609.1:c.1618+174A>G MANE Select ENSP00000483125.1:n.1618+174A>G
NM_207421.4:c.1618+174A>G MANE Select NP_997304.3:n.1618+174A>G
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