Canonical Allele Identifier: CA2708592787
Gene: PART1 HGNC NCBI

Linked Data

dbSNP Id: rs1023116394

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529248C>T , CM000667.2:g.60529248C>T GRCh38
NC_000005.9:g.59825075C>T , CM000667.1:g.59825075C>T GRCh37
NC_000005.8:g.59860832C>T NCBI36
NG_027957.2:g.82G>A

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.712-156C>T