ClinGen Allele Registry
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Canonical Allele Identifier:
CA444546239
Gene: PART1
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr5:g.59825278G>A (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.60529451G>A , CM000667.2:g.60529451G>A
GRCh38
NC_000005.9:g.59825278G>A , CM000667.1:g.59825278G>A
GRCh37
NC_000005.8:g.59861035G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_024617.1:n.759G>A
Search 100 bp 5'
Search 100 bp 3'