Canonical Allele Identifier: CA337465686
Gene: ZNF886P HGNC NCBI

Linked Data

dbSNP Id: rs72613054
MyVariant Identifiers: chrY:g.22166455G>T (hg19) chrY:g.20004569G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20004569G>T , CM000686.2:g.20004569G>T GRCh38
NC_000024.9:g.22166455G>T , CM000686.1:g.22166455G>T GRCh37
NC_000024.8:g.20625843G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000450781.1:n.208+1171C>A
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