Canonical Allele Identifier: CA1549819807
Gene: PART1 HGNC NCBI

Linked Data

dbSNP Id: rs1561334690

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529380T>C , CM000667.2:g.60529380T>C GRCh38
NC_000005.9:g.59825207T>C , CM000667.1:g.59825207T>C GRCh37
NC_000005.8:g.59860964T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024617.1:n.712-24T>C