Canonical Allele Identifier: CA470400672
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs1840478671
MyVariant Identifiers: chr10:g.79540843T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781085T>C , CM000672.2:g.77781085T>C GRCh38
NC_000010.10:g.79540843T>C , CM000672.1:g.79540843T>C GRCh37
NC_000010.9:g.79210849T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.792A>G