Canonical Allele Identifier: CA444546132
Gene: PART1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.59825241A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529414A>C , CM000667.2:g.60529414A>C GRCh38
NC_000005.9:g.59825241A>C , CM000667.1:g.59825241A>C GRCh37
NC_000005.8:g.59860998A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.722A>C