Canonical Allele Identifier: CA444546153
Gene: PART1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.59825248G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529421G>T , CM000667.2:g.60529421G>T GRCh38
NC_000005.9:g.59825248G>T , CM000667.1:g.59825248G>T GRCh37
NC_000005.8:g.59861005G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024617.1:n.729G>T
Search 100 bp 5'
Search 100 bp 3'