Canonical Allele Identifier: CA470400329

Gene: IMPDH1P5

Linked Data

• gnomAD v4: 10-77780967-T-C
• MyVariant Identifiers: chr10:g.79540725T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77780967T>C , CM000672.2:g.77780967T>C	GRCh38
NC_000010.10:g.79540725T>C , CM000672.1:g.79540725T>C	GRCh37
NC_000010.9:g.79210731T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439688.1:n.910A>G