Canonical Allele Identifier: CA209781932

Gene: IMPDH1P5

Linked Data

• dbSNP Id: rs1054615169
• gnomAD v4: 10-77780661-C-G
• MyVariant Identifiers: chr10:g.79540419C>G (hg19) ; chr10:g.77780661C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77780661C>G , CM000672.2:g.77780661C>G	GRCh38
NC_000010.10:g.79540419C>G , CM000672.1:g.79540419C>G	GRCh37
NC_000010.9:g.79210425C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439688.1:n.1216G>C