Canonical Allele Identifier: CA470399661
Gene: IMPDH1P5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79540503A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77780745A>T , CM000672.2:g.77780745A>T GRCh38
NC_000010.10:g.79540503A>T , CM000672.1:g.79540503A>T GRCh37
NC_000010.9:g.79210509A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.1132T>A