Canonical Allele Identifier: CA1921409715
Gene: IMPDH1P5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781267C= , CM000672.2:g.77781267C= GRCh38
NC_000010.10:g.79541025C= , CM000672.1:g.79541025C= GRCh37
NC_000010.9:g.79211031C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.610G=