Canonical Allele Identifier: CA470399672

Gene: IMPDH1P5

Linked Data

• gnomAD v4: 10-77780748-G-T
• MyVariant Identifiers: chr10:g.79540506G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77780748G>T , CM000672.2:g.77780748G>T	GRCh38
NC_000010.10:g.79540506G>T , CM000672.1:g.79540506G>T	GRCh37
NC_000010.9:g.79210512G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439688.1:n.1129C>A