Canonical Allele Identifier: CA1549819692
Gene: PART1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529247T= , CM000667.2:g.60529247T= GRCh38
NC_000005.9:g.59825074T= , CM000667.1:g.59825074T= GRCh37
NC_000005.8:g.59860831T= NCBI36
NG_027957.2:g.83A=

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.712-157T=