ClinGen Allele Registry
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Canonical Allele Identifier:
CA470401326
Gene: IMPDH1P5
HGNC
NCBI
Linked Data
dbSNP Id:
rs1488174292
MyVariant Identifiers:
chr10:g.79541040T>A (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.77781282T>A , CM000672.2:g.77781282T>A
GRCh38
NC_000010.10:g.79541040T>A , CM000672.1:g.79541040T>A
GRCh37
NC_000010.9:g.79211046T>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000439688.1:n.595A>T
Search 100 bp 5'
Search 100 bp 3'