Canonical Allele Identifier: CA444546116
Gene: PART1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.59825235C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529408C>T , CM000667.2:g.60529408C>T GRCh38
NC_000005.9:g.59825235C>T , CM000667.1:g.59825235C>T GRCh37
NC_000005.8:g.59860992C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024617.1:n.716C>T