Canonical Allele Identifier: CA470401602
Gene: IMPDH1P5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79541135T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781377T>G , CM000672.2:g.77781377T>G GRCh38
NC_000010.10:g.79541135T>G , CM000672.1:g.79541135T>G GRCh37
NC_000010.9:g.79211141T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.500A>C
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