Canonical Allele Identifier: CA444546146
Gene: PART1 HGNC NCBI

Linked Data

dbSNP Id: rs1751261735
MyVariant Identifiers: chr5:g.59825246A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529419A>C , CM000667.2:g.60529419A>C GRCh38
NC_000005.9:g.59825246A>C , CM000667.1:g.59825246A>C GRCh37
NC_000005.8:g.59861003A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.727A>C