Canonical Allele Identifier: CA470399528

Gene: IMPDH1P5

Linked Data

• dbSNP Id: rs1840476205
• gnomAD v3: 10-77780707-A-G
• gnomAD v4: 10-77780707-A-G
• MyVariant Identifiers: chr10:g.79540465A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77780707A>G , CM000672.2:g.77780707A>G	GRCh38
NC_000010.10:g.79540465A>G , CM000672.1:g.79540465A>G	GRCh37
NC_000010.9:g.79210471A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439688.1:n.1170T>C