Canonical Allele Identifier: CA209782055

Gene: IMPDH1P5

Linked Data

• dbSNP Id: rs760198582
• gnomAD v2: 10-79540770-T-G
• gnomAD v3: 10-77781012-T-G
• gnomAD v4: 10-77781012-T-G
• MyVariant Identifiers: chr10:g.79540770T>G (hg19) ; chr10:g.77781012T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77781012T>G , CM000672.2:g.77781012T>G	GRCh38
NC_000010.10:g.79540770T>G , CM000672.1:g.79540770T>G	GRCh37
NC_000010.9:g.79210776T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439688.1:n.865A>C