Canonical Allele Identifier: CA470401657
Gene: IMPDH1P5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79541157G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781399G>A , CM000672.2:g.77781399G>A GRCh38
NC_000010.10:g.79541157G>A , CM000672.1:g.79541157G>A GRCh37
NC_000010.9:g.79211163G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.478C>T
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