Canonical Allele Identifier: CA668670382
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs1388105700

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781090del , CM000672.2:g.77781090del GRCh38
NC_000010.10:g.79540848del , CM000672.1:g.79540848del GRCh37
NC_000010.9:g.79210854del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000439688.1:n.787del