Canonical Allele Identifier: CA9835123
Gene: FER1L4 HGNC NCBI
COSMIC:
COSN15628214 (not active)
COSN15629041 (not active)
COSN15631562 (not active)
COSN15633610 (not active)
COSN15634481 (not active)
COSN15637023 (not active)
COSN15642028 (not active)
COSN15642816 (not active)
COSN15644498 (not active)
COSN15646996 (not active)
COSN17131860 (not active)
COSN26634591 (not active)
MyVariant.info:
GRCh38 chr20:g.35564866C>T
GRCh37 chr20:g.34152782C>T
gnomAD v2:
20:34152782 C / T
gnomAD v3:
20:35564866 C / T
gnomAD v4:
chr20-35564866-C-T
Joint Max Group AF 0.30221157 (MID)
Genomes Max Group AF 0.27201271 (SAS)
Exomes Max Group AF 0.30549019 (MID)
dbSNP:
2277862
JSON-LD

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
ENST00000674340.1:n.2026G>A
ENST00000674470.1:n.1353G>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
NR_119376.1:n.4574G>A
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