Canonical Allele Identifier: CA327608132
Gene: PTCHD1-AS HGNC NCBI

Linked Data

dbSNP Id: rs969724765
MyVariant Identifiers: chrX:g.23100375G>A (hg19) chrX:g.23082258G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.23082258G>A , CM000685.2:g.23082258G>A GRCh38
NC_000023.10:g.23100375G>A , CM000685.1:g.23100375G>A GRCh37
NC_000023.9:g.23010296G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_073010.1:n.260-18137C>T
NR_073010.2:n.260-18137C>T
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