Canonical Allele Identifier: CA444546157
Gene: PART1 HGNC NCBI

Linked Data

gnomAD v4: 5-60529423-A-G
MyVariant Identifiers: chr5:g.59825250A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529423A>G , CM000667.2:g.60529423A>G GRCh38
NC_000005.9:g.59825250A>G , CM000667.1:g.59825250A>G GRCh37
NC_000005.8:g.59861007A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024617.1:n.731A>G
Search 100 bp 5'
Search 100 bp 3'