Canonical Allele Identifier: CA1921409534
Gene: IMPDH1P5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77780692T= , CM000672.2:g.77780692T= GRCh38
NC_000010.10:g.79540450T= , CM000672.1:g.79540450T= GRCh37
NC_000010.9:g.79210456T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.1185A=