Canonical Allele Identifier: CA209781957

Gene: IMPDH1P5

Linked Data

• dbSNP Id: rs183554690
• gnomAD v2: 10-79540549-T-C
• gnomAD v3: 10-77780791-T-C
• gnomAD v4: 10-77780791-T-C
• MyVariant Identifiers: chr10:g.79540549T>C (hg19) ; chr10:g.77780791T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77780791T>C , CM000672.2:g.77780791T>C	GRCh38
NC_000010.10:g.79540549T>C , CM000672.1:g.79540549T>C	GRCh37
NC_000010.9:g.79210555T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439688.1:n.1086A>G