Canonical Allele Identifier: CA444546323

Gene: PART1

Linked Data

• gnomAD v2: 5-59825306-A-G
• MyVariant Identifiers: chr5:g.59825306A>G (hg19) ; chr5:g.60529479A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60529479A>G , CM000667.2:g.60529479A>G	GRCh38
NC_000005.9:g.59825306A>G , CM000667.1:g.59825306A>G	GRCh37
NC_000005.8:g.59861063A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_024617.1:n.787A>G