Canonical Allele Identifier: CA416409157
Gene: PADI6 HGNC NCBI

Linked Data

dbSNP Id: rs2075302582
MyVariant Identifiers: chr1:g.17728131T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17401635T>C , CM000663.2:g.17401635T>C GRCh38
NC_000001.10:g.17728131T>C , CM000663.1:g.17728131T>C GRCh37
NC_000001.9:g.17600718T>C NCBI36
NG_032943.1:g.34390T>C
NG_032943.2:g.34390T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000619609.1:c.*197T>C MANE Select ENSP00000483125.1:n.*197T>C
NM_207421.4:c.*197T>C MANE Select NP_997304.3:n.*197T>C
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