Canonical Allele Identifier: CA444546154
Gene: PART1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.59825249C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529422C>A , CM000667.2:g.60529422C>A GRCh38
NC_000005.9:g.59825249C>A , CM000667.1:g.59825249C>A GRCh37
NC_000005.8:g.59861006C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.730C>A