Canonical Allele Identifier: CA470399515
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs1377903140
gnomAD v4: 10-77780703-G-A
MyVariant Identifiers: chr10:g.79540461G>A (hg19) chr10:g.77780703G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77780703G>A , CM000672.2:g.77780703G>A GRCh38
NC_000010.10:g.79540461G>A , CM000672.1:g.79540461G>A GRCh37
NC_000010.9:g.79210467G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.1174C>T
Search 100 bp 5'
Search 100 bp 3'