Canonical Allele Identifier: CA470400989
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs1403650104
gnomAD v2: 10-79540931-A-G
MyVariant Identifiers: chr10:g.79540931A>G (hg19) chr10:g.77781173A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781173A>G , CM000672.2:g.77781173A>G GRCh38
NC_000010.10:g.79540931A>G , CM000672.1:g.79540931A>G GRCh37
NC_000010.9:g.79210937A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.704T>C
Search 100 bp 5'
Search 100 bp 3'