Canonical Allele Identifier: CA2589278473
Gene: RFTN1P1 HGNC NCBI

Linked Data

dbSNP Id: rs2124250398
gnomAD v3: Y-7736161-T-C
gnomAD v4: Y-7736161-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7736161T>C , CM000686.2:g.7736161T>C GRCh38
NC_000024.9:g.7604202T>C , CM000686.1:g.7604202T>C GRCh37
NC_000024.8:g.7664202T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651261.1:n.299-23064A>G
ENST00000455527.5:n.297-6321A>G