Canonical Allele Identifier: CA209782191
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs529344330
gnomAD v2: 10-79541147-C-T
gnomAD v3: 10-77781389-C-T
gnomAD v4: 10-77781389-C-T
MyVariant Identifiers: chr10:g.79541147C>T (hg19) chr10:g.77781389C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781389C>T , CM000672.2:g.77781389C>T GRCh38
NC_000010.10:g.79541147C>T , CM000672.1:g.79541147C>T GRCh37
NC_000010.9:g.79211153C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.488G>A
Search 100 bp 5'
Search 100 bp 3'