Canonical Allele Identifier: CA470401606
Gene: IMPDH1P5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79541137G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781379G>C , CM000672.2:g.77781379G>C GRCh38
NC_000010.10:g.79541137G>C , CM000672.1:g.79541137G>C GRCh37
NC_000010.9:g.79211143G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.498C>G