Canonical Allele Identifier: CA1549819732
Gene: PART1 HGNC NCBI

Linked Data

dbSNP Id: rs1751259763

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529290C>T , CM000667.2:g.60529290C>T GRCh38
NC_000005.9:g.59825117C>T , CM000667.1:g.59825117C>T GRCh37
NC_000005.8:g.59860874C>T NCBI36
NG_027957.2:g.40G>A

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.712-114C>T