Canonical Allele Identifier: CA470400081

Gene: IMPDH1P5

Linked Data

• MyVariant Identifiers: chr10:g.79540639T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77780881T>G , CM000672.2:g.77780881T>G	GRCh38
NC_000010.10:g.79540639T>G , CM000672.1:g.79540639T>G	GRCh37
NC_000010.9:g.79210645T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439688.1:n.996A>C