Canonical Allele Identifier: CA1921409696
Gene: IMPDH1P5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781222A= , CM000672.2:g.77781222A= GRCh38
NC_000010.10:g.79540980A= , CM000672.1:g.79540980A= GRCh37
NC_000010.9:g.79210986A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.655T=