Canonical Allele Identifier: CA470399937
Gene: IMPDH1P5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79540591A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77780833A>C , CM000672.2:g.77780833A>C GRCh38
NC_000010.10:g.79540591A>C , CM000672.1:g.79540591A>C GRCh37
NC_000010.9:g.79210597A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.1044T>G