Canonical Allele Identifier: CA444546377

Gene: PART1

Linked Data

• dbSNP Id: rs1040255815
• gnomAD v2: 5-59825325-C-A
• gnomAD v3: 5-60529498-C-A
• gnomAD v4: 5-60529498-C-A
• MyVariant Identifiers: chr5:g.59825325C>A (hg19) ; chr5:g.60529498C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60529498C>A , CM000667.2:g.60529498C>A	GRCh38
NC_000005.9:g.59825325C>A , CM000667.1:g.59825325C>A	GRCh37
NC_000005.8:g.59861082C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_024617.1:n.806C>A