Canonical Allele Identifier: CA519545195
Gene: PRKY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.7246640G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7378599G>A , CM000686.2:g.7378599G>A GRCh38
NC_000024.9:g.7246640G>A , CM000686.1:g.7246640G>A GRCh37
NC_000024.8:g.7306640G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000528056.5:n.4269G>A
NR_028062.1:n.4269G>A
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