Canonical Allele Identifier: CA119478145

Gene: PART1

Linked Data

• dbSNP Id: rs1023116394
• MyVariant Identifiers: chr5:g.59825075C>A (hg19) ; chr5:g.60529248C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.60529248C>A , CM000667.2:g.60529248C>A	GRCh38
NC_000005.9:g.59825075C>A , CM000667.1:g.59825075C>A	GRCh37
NC_000005.8:g.59860832C>A	NCBI36
NG_027957.2:g.82G>T

Transcript Alleles

HGVS	Amino-acid Change
NR_024617.1:n.712-156C>A