Canonical Allele Identifier: CA510323653
Gene: FER1L4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.34152792C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35564876C>T , CM000682.2:g.35564876C>T GRCh38
NC_000020.10:g.34152792C>T , CM000682.1:g.34152792C>T GRCh37
NC_000020.9:g.33616206C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000674340.1:n.2016G>A
ENST00000674470.1:n.1343G>A
ENST00000611673.4:n.1037G>A
ENST00000613061.4:n.1387G>A
ENST00000615531.4:n.4552G>A
ENST00000616711.4:n.1701G>A
ENST00000621044.4:n.665G>A
NR_119376.1:n.4564G>A