Canonical Allele Identifier: CA1921409633
Gene: IMPDH1P5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781012T= , CM000672.2:g.77781012T= GRCh38
NC_000010.10:g.79540770T= , CM000672.1:g.79540770T= GRCh37
NC_000010.9:g.79210776T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.865A=