Canonical Allele Identifier: CA470400189
Gene: IMPDH1P5 HGNC NCBI

Linked Data

dbSNP Id: rs2154574483
gnomAD v4: 10-77780919-T-C
MyVariant Identifiers: chr10:g.79540677T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77780919T>C , CM000672.2:g.77780919T>C GRCh38
NC_000010.10:g.79540677T>C , CM000672.1:g.79540677T>C GRCh37
NC_000010.9:g.79210683T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439688.1:n.958A>G
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