ClinGen Allele Registry
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Canonical Allele Identifier:
CA470401129
Gene: IMPDH1P5
HGNC
NCBI
Linked Data
dbSNP Id:
rs1418151946
gnomAD v3:
10-77781214-T-C
gnomAD v4:
10-77781214-T-C
MyVariant Identifiers:
chr10:g.79540972T>C (hg19)
chr10:g.77781214T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.77781214T>C , CM000672.2:g.77781214T>C
GRCh38
NC_000010.10:g.79540972T>C , CM000672.1:g.79540972T>C
GRCh37
NC_000010.9:g.79210978T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000439688.1:n.663A>G
Search 100 bp 5'
Search 100 bp 3'