Canonical Allele Identifier: CA470401324
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs1192043480
gnomAD v3: 10-77781281-A-G
gnomAD v4: 10-77781281-A-G
MyVariant Identifiers: chr10:g.79541039A>G (hg19) chr10:g.77781281A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781281A>G , CM000672.2:g.77781281A>G GRCh38
NC_000010.10:g.79541039A>G , CM000672.1:g.79541039A>G GRCh37
NC_000010.9:g.79211045A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.596T>C
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