Canonical Allele Identifier: CA510323660
Gene: FER1L4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.34152794G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35564878G>T , CM000682.2:g.35564878G>T GRCh38
NC_000020.10:g.34152794G>T , CM000682.1:g.34152794G>T GRCh37
NC_000020.9:g.33616208G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000674340.1:n.2014C>A
ENST00000674470.1:n.1341C>A
ENST00000611673.4:n.1035C>A
ENST00000613061.4:n.1385C>A
ENST00000615531.4:n.4550C>A
ENST00000616711.4:n.1699C>A
ENST00000621044.4:n.663C>A
NR_119376.1:n.4562C>A