Canonical Allele Identifier: CA1138926940
Gene: RFTN1P1 HGNC NCBI

Linked Data

dbSNP Id: rs2014257667
gnomAD v3: Y-7779280-C-T
gnomAD v4: Y-7779280-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7779280C>T , CM000686.2:g.7779280C>T GRCh38
NC_000024.9:g.7647321C>T , CM000686.1:g.7647321C>T GRCh37
NC_000024.8:g.7707321C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651261.1:n.115-2576G>A
ENST00000652723.1:n.1027-2576G>A
ENST00000442584.2:n.219-2252G>A