Canonical Allele Identifier: CA1549819901
Gene: PART1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529496C= , CM000667.2:g.60529496C= GRCh38
NC_000005.9:g.59825323C= , CM000667.1:g.59825323C= GRCh37
NC_000005.8:g.59861080C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.804C=