Canonical Allele Identifier: CA510323649
Gene: FER1L4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.34152791T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35564875T>A , CM000682.2:g.35564875T>A GRCh38
NC_000020.10:g.34152791T>A , CM000682.1:g.34152791T>A GRCh37
NC_000020.9:g.33616205T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000674340.1:n.2017A>T
ENST00000674470.1:n.1344A>T
ENST00000611673.4:n.1038A>T
ENST00000613061.4:n.1388A>T
ENST00000615531.4:n.4553A>T
ENST00000616711.4:n.1702A>T
ENST00000621044.4:n.666A>T
NR_119376.1:n.4565A>T