Canonical Allele Identifier: CA209782182

Gene: IMPDH1P5

Linked Data

• dbSNP Id: rs564090040
• gnomAD v2: 10-79541123-C-T
• gnomAD v3: 10-77781365-C-T
• gnomAD v4: 10-77781365-C-T
• MyVariant Identifiers: chr10:g.79541123C>T (hg19) ; chr10:g.77781365C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77781365C>T , CM000672.2:g.77781365C>T	GRCh38
NC_000010.10:g.79541123C>T , CM000672.1:g.79541123C>T	GRCh37
NC_000010.9:g.79211129C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439688.1:n.512G>A