Canonical Allele Identifier: CA2469952270
Gene: RFTN1P1 HGNC NCBI

Linked Data

dbSNP Id: rs2014181740

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7725941T>C , CM000686.2:g.7725941T>C GRCh38
NC_000024.9:g.7593982T>C , CM000686.1:g.7593982T>C GRCh37
NC_000024.8:g.7653982T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000651261.1:n.299-12844A>G
ENST00000455527.5:n.680+3516A>G