Canonical Allele Identifier: CA470400506

Gene: IMPDH1P5

Linked Data

• dbSNP Id: rs1211789276
• gnomAD v3: 10-77781028-G-C
• gnomAD v4: 10-77781028-G-C
• MyVariant Identifiers: chr10:g.79540786G>C (hg19) ; chr10:g.77781028G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.77781028G>C , CM000672.2:g.77781028G>C	GRCh38
NC_000010.10:g.79540786G>C , CM000672.1:g.79540786G>C	GRCh37
NC_000010.9:g.79210792G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439688.1:n.849C>G