Canonical Allele Identifier: CA470401088
Gene: IMPDH1P5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79540960T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781202T>A , CM000672.2:g.77781202T>A GRCh38
NC_000010.10:g.79540960T>A , CM000672.1:g.79540960T>A GRCh37
NC_000010.9:g.79210966T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.675A>T