Canonical Allele Identifier: CA1921409759
Gene: IMPDH1P5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781378A= , CM000672.2:g.77781378A= GRCh38
NC_000010.10:g.79541136A= , CM000672.1:g.79541136A= GRCh37
NC_000010.9:g.79211142A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.499T=