Canonical Allele Identifier: CA337593768
Gene: RFTN1P1 HGNC NCBI

Linked Data

dbSNP Id: rs971211608

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7718847T>C , CM000686.2:g.7718847T>C GRCh38
NC_000024.9:g.7586888T>C , CM000686.1:g.7586888T>C GRCh37
NC_000024.8:g.7646888T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651261.1:n.299-5750A>G
ENST00000455527.5:n.883+3009A>G