Canonical Allele Identifier: CA1131620224
Gene: PTCHD1-AS HGNC NCBI

Linked Data

dbSNP Id: rs1922426845
gnomAD v3: X-23082293-T-C
gnomAD v4: X-23082293-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.23082293T>C , CM000685.2:g.23082293T>C GRCh38
NC_000023.10:g.23100410T>C , CM000685.1:g.23100410T>C GRCh37
NC_000023.9:g.23010331T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_073010.1:n.260-18172A>G
NR_073010.2:n.260-18172A>G
Search 100 bp 5'
Search 100 bp 3'