Canonical Allele Identifier: CA1921409619
Gene: IMPDH1P5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77780971C= , CM000672.2:g.77780971C= GRCh38
NC_000010.10:g.79540729C= , CM000672.1:g.79540729C= GRCh37
NC_000010.9:g.79210735C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.906G=