Canonical Allele Identifier: CA1131620209
Gene: PTCHD1-AS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.23082185T>C , CM000685.2:g.23082185T>C GRCh38
NC_000023.10:g.23100302T>C , CM000685.1:g.23100302T>C GRCh37
NC_000023.9:g.23010223T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_073010.1:n.260-18064A>G
NR_073010.2:n.260-18064A>G