Canonical Allele Identifier: CA1139017759
Gene: RFTN1P1 HGNC NCBI

Linked Data

gnomAD v3: Y-7736190-C-T
gnomAD v4: Y-7736190-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7736190C>T , CM000686.2:g.7736190C>T GRCh38
NC_000024.9:g.7604231C>T , CM000686.1:g.7604231C>T GRCh37
NC_000024.8:g.7664231C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651261.1:n.299-23093G>A
ENST00000455527.5:n.297-6350G>A