Canonical Allele Identifier: CA470400429
Gene: IMPDH1P5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79540760T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781002T>A , CM000672.2:g.77781002T>A GRCh38
NC_000010.10:g.79540760T>A , CM000672.1:g.79540760T>A GRCh37
NC_000010.9:g.79210766T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.875A>T