Canonical Allele Identifier: CA119478154

Gene: PART1

Linked Data

• dbSNP Id: rs545089764
• gnomAD v2: 5-59825157-G-T
• gnomAD v3: 5-60529330-G-T
• gnomAD v4: 5-60529330-G-T
• MyVariant Identifiers: chr5:g.59825157G>T (hg19) ; chr5:g.60529330G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60529330G>T , CM000667.2:g.60529330G>T	GRCh38
NC_000005.9:g.59825157G>T , CM000667.1:g.59825157G>T	GRCh37
NC_000005.8:g.59860914G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_024617.1:n.712-74G>T