Canonical Allele Identifier: CA470399484
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs1840476026
gnomAD v4: 10-77780692-T-C
MyVariant Identifiers: chr10:g.79540450T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77780692T>C , CM000672.2:g.77780692T>C GRCh38
NC_000010.10:g.79540450T>C , CM000672.1:g.79540450T>C GRCh37
NC_000010.9:g.79210456T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.1185A>G
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