Canonical Allele Identifier: CA510323716
Gene: FER1L4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.34152814G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35564898G>C , CM000682.2:g.35564898G>C GRCh38
NC_000020.10:g.34152814G>C , CM000682.1:g.34152814G>C GRCh37
NC_000020.9:g.33616228G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000674340.1:n.1994C>G
ENST00000674470.1:n.1321C>G
ENST00000611673.4:n.1015C>G
ENST00000613061.4:n.1365C>G
ENST00000615531.4:n.4530C>G
ENST00000616711.4:n.1679C>G
ENST00000621044.4:n.643C>G
NR_119376.1:n.4542C>G