Canonical Allele Identifier: CA2469950969
Gene: RFTN1P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7702870C= , CM000686.2:g.7702870C= GRCh38
NC_000024.9:g.7570911C= , CM000686.1:g.7570911C= GRCh37
NC_000024.8:g.7630911C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651261.1:n.677-1607G=