Canonical Allele Identifier: CA209781961
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs984635517
gnomAD v3: 10-77780846-C-CT
gnomAD v4: 10-77780846-C-CT
MyVariant Identifiers: chr10:g.79540604_79540605insT (hg19) chr10:g.77780846_77780847insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77780847dup , CM000672.2:g.77780847dup GRCh38
NC_000010.10:g.79540605dup , CM000672.1:g.79540605dup GRCh37
NC_000010.9:g.79210611dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.1030dup
Search 100 bp 5'
Search 100 bp 3'