Canonical Allele Identifier: CA209781947
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs549858655
gnomAD v3: 10-77780730-G-A
gnomAD v4: 10-77780730-G-A
MyVariant Identifiers: chr10:g.79540488G>A (hg19) chr10:g.77780730G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77780730G>A , CM000672.2:g.77780730G>A GRCh38
NC_000010.10:g.79540488G>A , CM000672.1:g.79540488G>A GRCh37
NC_000010.9:g.79210494G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.1147C>T
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