Canonical Allele Identifier: CA2361707841
Gene: FER1L4 HGNC NCBI

Linked Data

dbSNP Id: rs2064786590

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35564973G>A , CM000682.2:g.35564973G>A GRCh38
NC_000020.10:g.34152889G>A , CM000682.1:g.34152889G>A GRCh37
NC_000020.9:g.33616303G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000674340.1:n.1974-55C>T
ENST00000674470.1:n.1301-55C>T
ENST00000611673.4:n.995-55C>T
ENST00000613061.4:n.1345-55C>T
ENST00000615531.4:n.4510-55C>T
ENST00000616711.4:n.1659-55C>T
ENST00000621044.4:n.623-55C>T
NR_119376.1:n.4522-55C>T