Canonical Allele Identifier: CA1549819832
Gene: PART1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529419A= , CM000667.2:g.60529419A= GRCh38
NC_000005.9:g.59825246A= , CM000667.1:g.59825246A= GRCh37
NC_000005.8:g.59861003A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.727A=