Canonical Allele Identifier: CA444546156
Gene: PART1 HGNC NCBI

Linked Data

gnomAD v4: 5-60529422-C-T
MyVariant Identifiers: chr5:g.59825249C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529422C>T , CM000667.2:g.60529422C>T GRCh38
NC_000005.9:g.59825249C>T , CM000667.1:g.59825249C>T GRCh37
NC_000005.8:g.59861006C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.730C>T
Search 100 bp 5'
Search 100 bp 3'