Canonical Allele Identifier: CA337725467
Gene: SFPQP1 HGNC NCBI

Linked Data

dbSNP Id: rs867806572
MyVariant Identifiers: chrY:g.15202430C>T (hg19) chrY:g.13090516C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13090516C>T , CM000686.2:g.13090516C>T GRCh38
NC_000024.9:g.15202430C>T , CM000686.1:g.15202430C>T GRCh37
NC_000024.8:g.13711824C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000446621.1:n.556-4059C>T
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