Canonical Allele Identifier: CA510323391
Gene: FER1L4 HGNC NCBI

Linked Data

dbSNP Id: rs1372471457

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35564786G>A , CM000682.2:g.35564786G>A GRCh38
NC_000020.10:g.34152702G>A , CM000682.1:g.34152702G>A GRCh37
NC_000020.9:g.33616116G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000674340.1:n.2106C>T
ENST00000674470.1:n.1433C>T
ENST00000611673.4:n.1127C>T
ENST00000613061.4:n.1477C>T
ENST00000615531.4:n.4642C>T
ENST00000616711.4:n.1791C>T
ENST00000621044.4:n.755C>T
NR_119376.1:n.4654C>T