Canonical Allele Identifier: CA209782141
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs913430183

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781256C>A , CM000672.2:g.77781256C>A GRCh38
NC_000010.10:g.79541014C>A , CM000672.1:g.79541014C>A GRCh37
NC_000010.9:g.79211020C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.621G>T