Canonical Allele Identifier: CA519545947
Gene: PRKY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.7246733T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7378692T>C , CM000686.2:g.7378692T>C GRCh38
NC_000024.9:g.7246733T>C , CM000686.1:g.7246733T>C GRCh37
NC_000024.8:g.7306733T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000528056.5:n.4362T>C
NR_028062.1:n.4362T>C