Canonical Allele Identifier: CA470401561
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs1453061440
gnomAD v2: 10-79541120-T-G
gnomAD v3: 10-77781362-T-G
gnomAD v4: 10-77781362-T-G
MyVariant Identifiers: chr10:g.79541120T>G (hg19) chr10:g.77781362T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781362T>G , CM000672.2:g.77781362T>G GRCh38
NC_000010.10:g.79541120T>G , CM000672.1:g.79541120T>G GRCh37
NC_000010.9:g.79211126T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.515A>C
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