Canonical Allele Identifier: CA470400412

Gene: IMPDH1P5

Linked Data

• gnomAD v4: 10-77780996-C-G
• MyVariant Identifiers: chr10:g.79540754C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77780996C>G , CM000672.2:g.77780996C>G	GRCh38
NC_000010.10:g.79540754C>G , CM000672.1:g.79540754C>G	GRCh37
NC_000010.9:g.79210760C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000439688.1:n.881G>C