Canonical Allele Identifier: CA1549819700
Gene: PART1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529252C= , CM000667.2:g.60529252C= GRCh38
NC_000005.9:g.59825079C= , CM000667.1:g.59825079C= GRCh37
NC_000005.8:g.59860836C= NCBI36
NG_027957.2:g.78G=

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.712-152C=