Canonical Allele Identifier: CA119478159
Gene: PART1 HGNC NCBI

Linked Data

dbSNP Id: rs768160947

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529373A>G , CM000667.2:g.60529373A>G GRCh38
NC_000005.9:g.59825200A>G , CM000667.1:g.59825200A>G GRCh37
NC_000005.8:g.59860957A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024617.1:n.712-31A>G