Canonical Allele Identifier: CA510323732
Gene: FER1L4 HGNC NCBI

Linked Data

dbSNP Id: rs2064786060
gnomAD v4: 20-35564904-C-A
MyVariant Identifiers: chr20:g.34152820C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35564904C>A , CM000682.2:g.35564904C>A GRCh38
NC_000020.10:g.34152820C>A , CM000682.1:g.34152820C>A GRCh37
NC_000020.9:g.33616234C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000674340.1:n.1988G>T
ENST00000674470.1:n.1315G>T
ENST00000611673.4:n.1009G>T
ENST00000613061.4:n.1359G>T
ENST00000615531.4:n.4524G>T
ENST00000616711.4:n.1673G>T
ENST00000621044.4:n.637G>T
NR_119376.1:n.4536G>T
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