Canonical Allele Identifier: CA327608130
Gene: PTCHD1-AS HGNC NCBI

Linked Data

dbSNP Id: rs16982419
gnomAD v2: X-23100345-C-T
gnomAD v3: X-23082228-C-T
gnomAD v4: X-23082228-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.23082228C>T , CM000685.2:g.23082228C>T GRCh38
NC_000023.10:g.23100345C>T , CM000685.1:g.23100345C>T GRCh37
NC_000023.9:g.23010266C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_073010.1:n.260-18107G>A
NR_073010.2:n.260-18107G>A