Canonical Allele Identifier: CA470401451
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs1216671450
gnomAD v3: 10-77781324-C-T
gnomAD v4: 10-77781324-C-T
MyVariant Identifiers: chr10:g.79541082C>T (hg19) chr10:g.77781324C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781324C>T , CM000672.2:g.77781324C>T GRCh38
NC_000010.10:g.79541082C>T , CM000672.1:g.79541082C>T GRCh37
NC_000010.9:g.79211088C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.553G>A
Search 100 bp 5'
Search 100 bp 3'