Canonical Allele Identifier: CA519546021
Gene: PRKY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.7246739A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7378698A>C , CM000686.2:g.7378698A>C GRCh38
NC_000024.9:g.7246739A>C , CM000686.1:g.7246739A>C GRCh37
NC_000024.8:g.7306739A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000528056.5:n.4368A>C
NR_028062.1:n.4368A>C
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