Canonical Allele Identifier: CA1921409642
Gene: IMPDH1P5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781063A= , CM000672.2:g.77781063A= GRCh38
NC_000010.10:g.79540821A= , CM000672.1:g.79540821A= GRCh37
NC_000010.9:g.79210827A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.814T=