Canonical Allele Identifier: CA337593769
Gene: RFTN1P1 HGNC NCBI

Linked Data

dbSNP Id: rs111517397
gnomAD v3: Y-7718878-C-T
gnomAD v4: Y-7718878-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7718878C>T , CM000686.2:g.7718878C>T GRCh38
NC_000024.9:g.7586919C>T , CM000686.1:g.7586919C>T GRCh37
NC_000024.8:g.7646919C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651261.1:n.299-5781G>A
ENST00000455527.5:n.883+2978G>A