Canonical Allele Identifier: CA444546120
Gene: PART1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.59825237T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529410T>A , CM000667.2:g.60529410T>A GRCh38
NC_000005.9:g.59825237T>A , CM000667.1:g.59825237T>A GRCh37
NC_000005.8:g.59860994T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024617.1:n.718T>A