Canonical Allele Identifier: CA470399792

Gene: IMPDH1P5

Linked Data

• gnomAD v4: 10-77780783-A-C
• MyVariant Identifiers: chr10:g.79540541A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77780783A>C , CM000672.2:g.77780783A>C	GRCh38
NC_000010.10:g.79540541A>C , CM000672.1:g.79540541A>C	GRCh37
NC_000010.9:g.79210547A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439688.1:n.1094T>G