Canonical Allele Identifier: CA470401505
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs1840480970
MyVariant Identifiers: chr10:g.79541101A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781343A>G , CM000672.2:g.77781343A>G GRCh38
NC_000010.10:g.79541101A>G , CM000672.1:g.79541101A>G GRCh37
NC_000010.9:g.79211107A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.534T>C