Canonical Allele Identifier: CA18661134
Gene: PADI6 HGNC NCBI

Linked Data

dbSNP Id: rs1010050152
gnomAD v2: 1-17728118-TA-T
gnomAD v3: 1-17401622-TA-T
gnomAD v4: 1-17401622-TA-T
MyVariant Identifiers: chr1:g.17728119del (hg19) chr1:g.17401623del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17401623del , CM000663.2:g.17401623del GRCh38
NC_000001.10:g.17728119del , CM000663.1:g.17728119del GRCh37
NC_000001.9:g.17600706del NCBI36
NG_032943.1:g.34378del
NG_032943.2:g.34378del

Transcript Alleles

HGVS Amino-acid Change
ENST00000619609.1:c.*185del MANE Select ENSP00000483125.1:n.*185del
NM_207421.4:c.*185del MANE Select NP_997304.3:n.*185del
Search 100 bp 5'
Search 100 bp 3'