Canonical Allele Identifier: CA9835125
Gene: FER1L4 HGNC NCBI

Linked Data

dbSNP Id: rs771412663

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35564883G>A , CM000682.2:g.35564883G>A GRCh38
NC_000020.10:g.34152799G>A , CM000682.1:g.34152799G>A GRCh37
NC_000020.9:g.33616213G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000674340.1:n.2009C>T
ENST00000674470.1:n.1336C>T
ENST00000611673.4:n.1030C>T
ENST00000613061.4:n.1380C>T
ENST00000615531.4:n.4545C>T
ENST00000616711.4:n.1694C>T
ENST00000621044.4:n.658C>T
NR_119376.1:n.4557C>T