Canonical Allele Identifier: CA668670251
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs1484170392

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77780814del , CM000672.2:g.77780814del GRCh38
NC_000010.10:g.79540572del , CM000672.1:g.79540572del GRCh37
NC_000010.9:g.79210578del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.1065del