Canonical Allele Identifier: CA1139008261
Gene: RFTN1P1 HGNC NCBI

Linked Data

dbSNP Id: rs2014146746
gnomAD v3: Y-7702797-A-C
gnomAD v4: Y-7702797-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7702797A>C , CM000686.2:g.7702797A>C GRCh38
NC_000024.9:g.7570838A>C , CM000686.1:g.7570838A>C GRCh37
NC_000024.8:g.7630838A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651261.1:n.677-1534T>G