Canonical Allele Identifier: CA812700146

Gene: PART1

Linked Data

• dbSNP Id: rs1156536885
• MyVariant Identifiers: chr5:g.59825135G>T (hg19) ; chr5:g.60529308G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60529308G>T , CM000667.2:g.60529308G>T	GRCh38
NC_000005.9:g.59825135G>T , CM000667.1:g.59825135G>T	GRCh37
NC_000005.8:g.59860892G>T	NCBI36
NG_027957.2:g.22C>A

Transcript Alleles

HGVS	Amino-acid Change
NR_024617.1:n.712-96G>T