Canonical Allele Identifier: CA9835123
Gene: FER1L4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2277862

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35564866C>T , CM000682.2:g.35564866C>T GRCh38
NC_000020.10:g.34152782C>T , CM000682.1:g.34152782C>T GRCh37
NC_000020.9:g.33616196C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_119376.1:n.4574G>A
ENST00000611673.4:n.1047G>A
ENST00000613061.4:n.1397G>A
ENST00000615531.4:n.4562G>A
ENST00000616711.4:n.1711G>A
ENST00000621044.4:n.675G>A