Canonical Allele Identifier: CA470400720
Gene: IMPDH1P5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.79540856G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781098G>C , CM000672.2:g.77781098G>C GRCh38
NC_000010.10:g.79540856G>C , CM000672.1:g.79540856G>C GRCh37
NC_000010.9:g.79210862G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.779C>G