Canonical Allele Identifier: CA470399980
Gene: IMPDH1P5 HGNC NCBI

Linked Data

gnomAD v4: 10-77780847-T-C
MyVariant Identifiers: chr10:g.79540605T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77780847T>C , CM000672.2:g.77780847T>C GRCh38
NC_000010.10:g.79540605T>C , CM000672.1:g.79540605T>C GRCh37
NC_000010.9:g.79210611T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.1030A>G
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