Canonical Allele Identifier: CA812700155

Gene: PART1

Linked Data

• dbSNP Id: rs1200539578
• gnomAD v3: 5-60529322-C-T
• gnomAD v4: 5-60529322-C-T
• MyVariant Identifiers: chr5:g.59825149C>T (hg19) ; chr5:g.60529322C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60529322C>T , CM000667.2:g.60529322C>T	GRCh38
NC_000005.9:g.59825149C>T , CM000667.1:g.59825149C>T	GRCh37
NC_000005.8:g.59860906C>T	NCBI36
NG_027957.2:g.8G>A

Transcript Alleles

HGVS	Amino-acid Change
NR_024617.1:n.712-82C>T