Canonical Allele Identifier: CA519545962
Gene: PRKY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.7246734A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7378693A>T , CM000686.2:g.7378693A>T GRCh38
NC_000024.9:g.7246734A>T , CM000686.1:g.7246734A>T GRCh37
NC_000024.8:g.7306734A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000528056.5:n.4363A>T
NR_028062.1:n.4363A>T
Search 100 bp 5'
Search 100 bp 3'