Canonical Allele Identifier: CA743918738
Gene: FER1L4 HGNC NCBI

Linked Data

dbSNP Id: rs1455353593

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35564938A>T , CM000682.2:g.35564938A>T GRCh38
NC_000020.10:g.34152854A>T , CM000682.1:g.34152854A>T GRCh37
NC_000020.9:g.33616268A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000674340.1:n.1974-20T>A
ENST00000674470.1:n.1301-20T>A
ENST00000611673.4:n.995-20T>A
ENST00000613061.4:n.1345-20T>A
ENST00000615531.4:n.4510-20T>A
ENST00000616711.4:n.1659-20T>A
ENST00000621044.4:n.623-20T>A
NR_119376.1:n.4522-20T>A