Canonical Allele Identifier: CA2673955732
Gene: PART1 HGNC NCBI

Linked Data

gnomAD v4: 5-60529335-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529335G>T , CM000667.2:g.60529335G>T GRCh38
NC_000005.9:g.59825162G>T , CM000667.1:g.59825162G>T GRCh37
NC_000005.8:g.59860919G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.712-69G>T