Canonical Allele Identifier: CA13195716

Gene: IMPDH1P5

Linked Data

• dbSNP Id: rs148143595
• gnomAD v2: 10-79540963-G-A
• gnomAD v3: 10-77781205-G-A
• gnomAD v4: 10-77781205-G-A
• MyVariant Identifiers: chr10:g.79540963G>A (hg19) ; chr10:g.77781205G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77781205G>A , CM000672.2:g.77781205G>A	GRCh38
NC_000010.10:g.79540963G>A , CM000672.1:g.79540963G>A	GRCh37
NC_000010.9:g.79210969G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439688.1:n.672C>T