Canonical Allele Identifier: CA470400661

Gene: IMPDH1P5

Linked Data

• gnomAD v4: 10-77781081-T-C
• MyVariant Identifiers: chr10:g.79540839T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77781081T>C , CM000672.2:g.77781081T>C	GRCh38
NC_000010.10:g.79540839T>C , CM000672.1:g.79540839T>C	GRCh37
NC_000010.9:g.79210845T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439688.1:n.796A>G