ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA470399882
Gene: IMPDH1P5
HGNC
NCBI
Linked Data
dbSNP Id:
rs1240193182
gnomAD v3:
10-77780814-G-A
gnomAD v4:
10-77780814-G-A
MyVariant Identifiers:
chr10:g.79540572G>A (hg19)
chr10:g.77780814G>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.77780814G>A , CM000672.2:g.77780814G>A
GRCh38
NC_000010.10:g.79540572G>A , CM000672.1:g.79540572G>A
GRCh37
NC_000010.9:g.79210578G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000439688.1:n.1063C>T
Search 100 bp 5'
Search 100 bp 3'