Canonical Allele Identifier: CA470399384
Gene: IMPDH1P5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79540415G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77780657G>T , CM000672.2:g.77780657G>T GRCh38
NC_000010.10:g.79540415G>T , CM000672.1:g.79540415G>T GRCh37
NC_000010.9:g.79210421G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.1220C>A