Canonical Allele Identifier: CA874020018
Gene: PTCHD1-AS HGNC NCBI

Linked Data

dbSNP Id: rs1338771574
MyVariant Identifiers: chrX:g.23100355G>C (hg19) chrX:g.23082238G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.23082238G>C , CM000685.2:g.23082238G>C GRCh38
NC_000023.10:g.23100355G>C , CM000685.1:g.23100355G>C GRCh37
NC_000023.9:g.23010276G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_073010.1:n.260-18117C>G
NR_073010.2:n.260-18117C>G
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