ClinGen Allele Registry
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Canonical Allele Identifier:
CA880344958
Gene: SFPQP1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1453822834
MyVariant Identifiers:
chrY:g.15202549G>C (hg19)
chrY:g.13090635G>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.13090635G>C , CM000686.2:g.13090635G>C
GRCh38
NC_000024.9:g.15202549G>C , CM000686.1:g.15202549G>C
GRCh37
NC_000024.8:g.13711943G>C
NCBI36
Transcript Alleles
HGVS
Amino-acid change
ENST00000446621.1:n.556-3940G>C
Search 100 bp 5'
Search 100 bp 3'