Canonical Allele Identifier: CA444546367
Gene: PART1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.59825321G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529494G>C , CM000667.2:g.60529494G>C GRCh38
NC_000005.9:g.59825321G>C , CM000667.1:g.59825321G>C GRCh37
NC_000005.8:g.59861078G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.802G>C
Search 100 bp 5'
Search 100 bp 3'