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Canonical Allele Identifier:
CA12141737
Gene: PART1
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr5:g.60529473T>C
GRCh37
chr5:g.59825300T>C
Linked Data - Sequence & Population
gnomAD v2:
5:59825300 T / C
gnomAD v3:
5:60529473 T / C
gnomAD v4:
chr5-60529473-T-C
Joint Max Group AF
0.53739486 (EAS)
Genomes Max Group AF
0.53739486 (EAS)
Linked Data - NCBI & NCI
dbSNP:
26949
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.60529473T>C , CM000667.2:g.60529473T>C
GRCh38
NC_000005.9:g.59825300T>C , CM000667.1:g.59825300T>C
GRCh37
NC_000005.8:g.59861057T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_024617.1:n.781T>C
Search 100 bp 5'
Search 100 bp 3'