Canonical Allele Identifier: CA470401532

Gene: IMPDH1P5

Linked Data

• gnomAD v4: 10-77781352-C-A
• MyVariant Identifiers: chr10:g.79541110C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77781352C>A , CM000672.2:g.77781352C>A	GRCh38
NC_000010.10:g.79541110C>A , CM000672.1:g.79541110C>A	GRCh37
NC_000010.9:g.79211116C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439688.1:n.525G>T