Canonical Allele Identifier: CA470401543
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs1014752968
gnomAD v3: 10-77781356-T-C
gnomAD v4: 10-77781356-T-C
MyVariant Identifiers: chr10:g.79541114T>C (hg19) chr10:g.77781356T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781356T>C , CM000672.2:g.77781356T>C GRCh38
NC_000010.10:g.79541114T>C , CM000672.1:g.79541114T>C GRCh37
NC_000010.9:g.79211120T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.521A>G
Search 100 bp 5'
Search 100 bp 3'