Canonical Allele Identifier: CA1138925259
Gene: RFTN1P1 HGNC NCBI

Linked Data

gnomAD v3: Y-7777391-G-C
gnomAD v4: Y-7777391-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7777391G>C , CM000686.2:g.7777391G>C GRCh38
NC_000024.9:g.7645432G>C , CM000686.1:g.7645432G>C GRCh37
NC_000024.8:g.7705432G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651261.1:n.115-687C>G
ENST00000652723.1:n.1027-687C>G
ENST00000442584.2:n.219-363C>G