Canonical Allele Identifier: CA2419527122
Gene: PTCHD1-AS HGNC NCBI

Linked Data

dbSNP Id: rs1922424158

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.23082174T>C , CM000685.2:g.23082174T>C GRCh38
NC_000023.10:g.23100291T>C , CM000685.1:g.23100291T>C GRCh37
NC_000023.9:g.23010212T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_073010.1:n.260-18053A>G
NR_073010.2:n.260-18053A>G