Canonical Allele Identifier: CA1921409729
Gene: IMPDH1P5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781298T= , CM000672.2:g.77781298T= GRCh38
NC_000010.10:g.79541056T= , CM000672.1:g.79541056T= GRCh37
NC_000010.9:g.79211062T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.579A=