Canonical Allele Identifier: CA880385775
Gene: RFTN1P1 HGNC NCBI

Linked Data

dbSNP Id: rs1242969709

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7725936A>C , CM000686.2:g.7725936A>C GRCh38
NC_000024.9:g.7593977A>C , CM000686.1:g.7593977A>C GRCh37
NC_000024.8:g.7653977A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651261.1:n.299-12839T>G
ENST00000455527.5:n.680+3521T>G