Canonical Allele Identifier: CA519545927
Gene: PRKY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.7246730A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7378689A>C , CM000686.2:g.7378689A>C GRCh38
NC_000024.9:g.7246730A>C , CM000686.1:g.7246730A>C GRCh37
NC_000024.8:g.7306730A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000528056.5:n.4359A>C
NR_028062.1:n.4359A>C