ClinGen Allele Registry
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Canonical Allele Identifier:
CA880344963
Gene: SFPQP1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1339045674
MyVariant Identifiers:
chrY:g.15202559A>G (hg19)
chrY:g.13090645A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.13090645A>G , CM000686.2:g.13090645A>G
GRCh38
NC_000024.9:g.15202559A>G , CM000686.1:g.15202559A>G
GRCh37
NC_000024.8:g.13711953A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000446621.1:n.556-3930A>G
Search 100 bp 5'
Search 100 bp 3'