Canonical Allele Identifier: CA1549819801
Gene: PART1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529375T= , CM000667.2:g.60529375T= GRCh38
NC_000005.9:g.59825202T= , CM000667.1:g.59825202T= GRCh37
NC_000005.8:g.59860959T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024617.1:n.712-29T=