Canonical Allele Identifier: CA519545183
Gene: PRKY HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.7246637T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7378596T>G , CM000686.2:g.7378596T>G GRCh38
NC_000024.9:g.7246637T>G , CM000686.1:g.7246637T>G GRCh37
NC_000024.8:g.7306637T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000528056.5:n.4266T>G
NR_028062.1:n.4266T>G
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