Canonical Allele Identifier: CA444546197
Gene: PART1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.59825263A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529436A>T , CM000667.2:g.60529436A>T GRCh38
NC_000005.9:g.59825263A>T , CM000667.1:g.59825263A>T GRCh37
NC_000005.8:g.59861020A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.744A>T