Canonical Allele Identifier: CA559966751

Gene: PART1

Linked Data

• dbSNP Id: rs1434981099
• gnomAD v2: 5-59825085-TG-T
• gnomAD v3: 5-60529258-TG-T
• gnomAD v4: 5-60529258-TG-T
• MyVariant Identifiers: chr5:g.59825086del (hg19) ; chr5:g.60529259del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60529262del , CM000667.2:g.60529262del	GRCh38
NC_000005.9:g.59825089del , CM000667.1:g.59825089del	GRCh37
NC_000005.8:g.59860846del	NCBI36
NG_027957.2:g.71del

Transcript Alleles

HGVS	Amino-acid Change
NR_024617.1:n.712-142del