Canonical Allele Identifier: CA444546130
Gene: PART1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.59825240T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529413T>C , CM000667.2:g.60529413T>C GRCh38
NC_000005.9:g.59825240T>C , CM000667.1:g.59825240T>C GRCh37
NC_000005.8:g.59860997T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024617.1:n.721T>C