Canonical Allele Identifier: CA2469952089
Gene: RFTN1P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7721262T= , CM000686.2:g.7721262T= GRCh38
NC_000024.9:g.7589303T= , CM000686.1:g.7589303T= GRCh37
NC_000024.8:g.7649303T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651261.1:n.299-8165A=
ENST00000455527.5:n.883+594A=