Canonical Allele Identifier: CA470400785

Gene: IMPDH1P5

Linked Data

• dbSNP Id: rs1164755540
• gnomAD v2: 10-79540875-C-T
• gnomAD v3: 10-77781117-C-T
• gnomAD v4: 10-77781117-C-T
• MyVariant Identifiers: chr10:g.79540875C>T (hg19) ; chr10:g.77781117C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77781117C>T , CM000672.2:g.77781117C>T	GRCh38
NC_000010.10:g.79540875C>T , CM000672.1:g.79540875C>T	GRCh37
NC_000010.9:g.79210881C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439688.1:n.760G>A