Canonical Allele Identifier: CA1139015299
Gene: RFTN1P1 HGNC NCBI

Linked Data

gnomAD v3: Y-7725881-G-A
gnomAD v4: Y-7725881-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7725881G>A , CM000686.2:g.7725881G>A GRCh38
NC_000024.9:g.7593922G>A , CM000686.1:g.7593922G>A GRCh37
NC_000024.8:g.7653922G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651261.1:n.299-12784C>T
ENST00000455527.5:n.680+3576C>T