Canonical Allele Identifier: CA2673955730
Gene: PART1 HGNC NCBI

Linked Data

gnomAD v4: 5-60529317-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529317T>C , CM000667.2:g.60529317T>C GRCh38
NC_000005.9:g.59825144T>C , CM000667.1:g.59825144T>C GRCh37
NC_000005.8:g.59860901T>C NCBI36
NG_027957.2:g.13A>G

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.712-87T>C