Canonical Allele Identifier: CA470399660

Gene: IMPDH1P5

Linked Data

• gnomAD v4: 10-77780745-A-G
• MyVariant Identifiers: chr10:g.79540503A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77780745A>G , CM000672.2:g.77780745A>G	GRCh38
NC_000010.10:g.79540503A>G , CM000672.1:g.79540503A>G	GRCh37
NC_000010.9:g.79210509A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439688.1:n.1132T>C