Canonical Allele Identifier: CA1549819780
Gene: PART1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529342A= , CM000667.2:g.60529342A= GRCh38
NC_000005.9:g.59825169A= , CM000667.1:g.59825169A= GRCh37
NC_000005.8:g.59860926A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.712-62A=