Canonical Allele Identifier: CA470399619
Gene: IMPDH1P5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79540491G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77780733G>C , CM000672.2:g.77780733G>C GRCh38
NC_000010.10:g.79540491G>C , CM000672.1:g.79540491G>C GRCh37
NC_000010.9:g.79210497G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.1144C>G
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