Canonical Allele Identifier: CA918712444
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs1568097833
gnomAD v4: 10-77781289-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781292del , CM000672.2:g.77781292del GRCh38
NC_000010.10:g.79541050del , CM000672.1:g.79541050del GRCh37
NC_000010.9:g.79211056del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.587del
Search 100 bp 5'
Search 100 bp 3'