Canonical Allele Identifier: CA470401521

Gene: IMPDH1P5

Linked Data

• dbSNP Id: rs1840481005
• gnomAD v4: 10-77781348-C-T
• MyVariant Identifiers: chr10:g.79541106C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77781348C>T , CM000672.2:g.77781348C>T	GRCh38
NC_000010.10:g.79541106C>T , CM000672.1:g.79541106C>T	GRCh37
NC_000010.9:g.79211112C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439688.1:n.529G>A