Canonical Allele Identifier: CA327608129
Gene: PTCHD1-AS HGNC NCBI

Linked Data

dbSNP Id: rs1013384889
MyVariant Identifiers: chrX:g.23100344A>G (hg19) chrX:g.23082227A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.23082227A>G , CM000685.2:g.23082227A>G GRCh38
NC_000023.10:g.23100344A>G , CM000685.1:g.23100344A>G GRCh37
NC_000023.9:g.23010265A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_073010.1:n.260-18106T>C
NR_073010.2:n.260-18106T>C
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