Canonical Allele Identifier: CA559966750

Gene: PART1

Linked Data

• dbSNP Id: rs1440935136
• gnomAD v2: 5-59825074-TC-T
• gnomAD v3: 5-60529247-TC-T
• gnomAD v4: 5-60529247-TC-T
• MyVariant Identifiers: chr5:g.59825075del (hg19) ; chr5:g.60529248del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60529252del , CM000667.2:g.60529252del	GRCh38
NC_000005.9:g.59825079del , CM000667.1:g.59825079del	GRCh37
NC_000005.8:g.59860836del	NCBI36
NG_027957.2:g.82del

Transcript Alleles

HGVS	Amino-acid Change
NR_024617.1:n.712-152del