Canonical Allele Identifier: CA470400090

Gene: IMPDH1P5

Linked Data

• dbSNP Id: rs1369193132
• gnomAD v2: 10-79540642-A-C
• gnomAD v3: 10-77780884-A-C
• gnomAD v4: 10-77780884-A-C
• MyVariant Identifiers: chr10:g.79540642A>C (hg19) ; chr10:g.77780884A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77780884A>C , CM000672.2:g.77780884A>C	GRCh38
NC_000010.10:g.79540642A>C , CM000672.1:g.79540642A>C	GRCh37
NC_000010.9:g.79210648A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439688.1:n.993T>G