Canonical Allele Identifier: CA470399902

Gene: IMPDH1P5

Linked Data

• gnomAD v4: 10-77780820-T-C
• MyVariant Identifiers: chr10:g.79540578T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77780820T>C , CM000672.2:g.77780820T>C	GRCh38
NC_000010.10:g.79540578T>C , CM000672.1:g.79540578T>C	GRCh37
NC_000010.9:g.79210584T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439688.1:n.1057A>G