Canonical Allele Identifier: CA444546283

Gene: PART1

Linked Data

• gnomAD v4: 5-60529466-T-A
• MyVariant Identifiers: chr5:g.59825293T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60529466T>A , CM000667.2:g.60529466T>A	GRCh38
NC_000005.9:g.59825293T>A , CM000667.1:g.59825293T>A	GRCh37
NC_000005.8:g.59861050T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_024617.1:n.774T>A