Canonical Allele Identifier: CA119478151
Gene: PART1 HGNC NCBI

Linked Data

dbSNP Id: rs956319926
MyVariant Identifiers: chr5:g.59825086G>A (hg19) chr5:g.60529259G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529259G>A , CM000667.2:g.60529259G>A GRCh38
NC_000005.9:g.59825086G>A , CM000667.1:g.59825086G>A GRCh37
NC_000005.8:g.59860843G>A NCBI36
NG_027957.2:g.71C>T

Transcript Alleles

HGVS Amino-acid Change
NR_024617.1:n.712-145G>A
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