Canonical Allele Identifier: CA470400080
Gene: IMPDH1P5 HGNC NCBI

Linked Data

COSMIC: COSN10073057
MyVariant Identifiers: chr10:g.79540639T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77780881T>A , CM000672.2:g.77780881T>A GRCh38
NC_000010.10:g.79540639T>A , CM000672.1:g.79540639T>A GRCh37
NC_000010.9:g.79210645T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.996A>T
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