ClinGen Allele Registry
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Canonical Allele Identifier:
CA15643710
Gene: IMPDH1P5
HGNC
NCBI
Linked Data
dbSNP Id:
rs1045957874
gnomAD v2:
10-79541024-A-G
gnomAD v3:
10-77781266-A-G
gnomAD v4:
10-77781266-A-G
MyVariant Identifiers:
chr10:g.79541024A>G (hg19)
chr10:g.77781266A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.77781266A>G , CM000672.2:g.77781266A>G
GRCh38
NC_000010.10:g.79541024A>G , CM000672.1:g.79541024A>G
GRCh37
NC_000010.9:g.79211030A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000439688.1:n.611T>C
Search 100 bp 5'
Search 100 bp 3'