Canonical Allele Identifier: CA470401491
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs1339630095
gnomAD v4: 10-77781338-G-A
MyVariant Identifiers: chr10:g.79541096G>A (hg19) chr10:g.77781338G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781338G>A , CM000672.2:g.77781338G>A GRCh38
NC_000010.10:g.79541096G>A , CM000672.1:g.79541096G>A GRCh37
NC_000010.9:g.79211102G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.539C>T
Search 100 bp 5'
Search 100 bp 3'