Canonical Allele Identifier: CA470400092
Gene: IMPDH1P5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79540642A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77780884A>G , CM000672.2:g.77780884A>G GRCh38
NC_000010.10:g.79540642A>G , CM000672.1:g.79540642A>G GRCh37
NC_000010.9:g.79210648A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.993T>C