Canonical Allele Identifier: CA337602694
Gene: PARP4P1 HGNC NCBI

Linked Data

dbSNP Id: rs66802889
MyVariant Identifiers: chrY:g.28771116G>C (hg19) chrY:g.26624969G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.26624969G>C , CM000686.2:g.26624969G>C GRCh38
NC_000024.9:g.28771116G>C , CM000686.1:g.28771116G>C GRCh37
NC_000024.8:g.27180504G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000435945.1:n.568-1303C>G
Search 100 bp 5'
Search 100 bp 3'