ClinGen Allele Registry
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Canonical Allele Identifier:
CA470400681
Gene: IMPDH1P5
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr10:g.79540845A>G (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.77781087A>G , CM000672.2:g.77781087A>G
GRCh38
NC_000010.10:g.79540845A>G , CM000672.1:g.79540845A>G
GRCh37
NC_000010.9:g.79210851A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000439688.1:n.790T>C
Search 100 bp 5'
Search 100 bp 3'