Canonical Allele Identifier: CA594710218
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs1349225393
gnomAD v2: 10-79540425-TAAG-T
gnomAD v3: 10-77780667-TAAG-T
gnomAD v4: 10-77780667-TAAG-T
MyVariant Identifiers: chr10:g.79540426_79540428del (hg19) chr10:g.77780668_77780670del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77780674_77780676del , CM000672.2:g.77780674_77780676del GRCh38
NC_000010.10:g.79540432_79540434del , CM000672.1:g.79540432_79540434del GRCh37
NC_000010.9:g.79210438_79210440del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.1207_1209del
Search 100 bp 5'
Search 100 bp 3'